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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

S. NO. 1 (RADIOLOGY EQUIPMENT)


1.1 MOBILE X-RAY MACHINE
Clinical Specialty Radiology, ICU, HDU, Wards
Generic Name Mobile X-Ray Machine/Portable X-Ray Machine/Transport X-Ray Machine
Clinical Purpose Mobile X-Ray System are often used to perform chest radiography to patients who cannot be
moved to the Radiology department. An X-Ray mobile system consist of a motorized drive,
compact wheelbase that includes the generator, an x-ray tube attached to a positioning column
and an exposure control panel.
TECHNICAL SPECIFICATIONS
1. GENERATOR
 The highest high-frequency high-voltage generator 20KHz or better
 High control precision, KV, mA real-time control.
 Protection circuit to control the generator temperature, overheating, overcurrent, overvoltage,
tube overload protection
 Generator with wide working voltage range
 Power: 30KW or better
 Tube Current: 10mA~400mA or better
 mAs: 0.1~300mAs or better
 Exposure time: 1ms~8 sec or better
 Exposure voltage kV: 40-150kV or better
 APR: 1000 or as per manufacturer.
 Power Input: 100V-240 AC Single phase, 50/60Hz
2. X-RAY TUBE
 Rotating anode X-ray tube
 Anode heat storage capacity 140kHU or better
 Focal spot: dual focus 0.6 mm/1.2 mm or better
 Tube Voltage: 40~ 150kV or better
 Inherent filtration: 0.9mmAl or better
3. Movements
 Tube assembly vertical plane rotation angle: -90°~90° or better
 Tube assembly horizontal axis rotation angle: -90°~90° or better
 Tube assembly tilting angle: -30°~90° or better
4. BATTERY BACKUP
 Battery backup of 100 exposures and can drive 50 KM was changed to 5Km routine usage
when fully charged
 Charging time: 3.5h or better
 The sensor in the front to automatically stops the device if a slight pressure is detected
 Dual way braking
 Unit movement driven by power or manual
NOTE:
 The system should be FDA/CE/JIS/MHLW approved. One Certificate mandatory.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PNRA Registration will be responsibility of the supplier.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

1.2 128 SLICES WHOLE BODY COMPUTERIZED TOMOGRAPHY SCANNER


Clinical Specialty Radiology
Generic Name CT Scan Machine
Clinical Purpose The CT Scan machine works on principles of X Ray emission and then
retrieving the images through an array of multiple detectors, uses for taking
images of different parts of the body for further diagnosis.
TECHNICAL SPECIFICATIONS
Latest Generation Whole Body 128-Slices or more CT Scanner with Latest Clinical
Application Software
GANTRY:
Gantry bore to be at least 70cm or more.
Minimum gantry rotation speed to be at least 0.35sec for 128 slices per 360º rotation or
better.
Gantry tilt must be -24 º and +30 º or better. System to be capable of acquiring with gantry
tilting.
Two-way intercom system for patient operator communication shall be provided.
Dual Control (including tilt) of Gantry and table from the gantry housing and console.
Maximum Scan field of view to be at least 50 cm.
Detector width should be 38 mm or more enabling better patient coverage / rotation.
Special workflows & ability to program the scanner from the gantry display for special
emergency needs.
Maximum scan time 100sec or more for handling heavy patient load.
TUBE:
Heat storage capacity of at least 7.0MHU or more.
Anode heat dissipation of at least 1200kHU/min or better.
Dual focal tissus as per manufacturer
GENERATOR & DETECTOR:
High frequency type maximum power of at least 80kw or more.
80 to 135 kV range or better.
Being able to do 70 kV as Low kV technique to reduce Radiation Dose.
Tube current of 600mA or more with 5mA increments or smaller.
Automatic dose modulation hardware/software.
Low contrast detectability (LCD) calculated on a catphan ct phantom of 4mm or better
resolution with a CT number of 3HU (0.3%) contrast difference.
Spatial resolution of 20lp/cm at mtf 0% at reference or better.
Slice thickness/pixel size of 0.625mm or better.
Scan length of at least 1.7 meters in a single acquisition or longer.
Detector Rows: 64 or more
Detector Elements: 60,000 or more as per manufacturer.
Detector Width: 38mm or more
Must mention physical size of each detector element along with total number.
Isotropic resolution = or <0.30mm in standard and high-resolution modes.
Automated mA modulation according to patient size and tissue density.
Automated kV selection based on initial scanogram /spot scan.
PATIENT COUCH:
Single acquisition scans range of at least 1.7meter or longer.
Weight bearing capacity of minimum 200kg or more.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

Motorized control (form console and gantry) of table movements in horizontal and vertical
axis.
Scan with at least 0.25 mm accuracy/ reproducibility on a 200 kg patient.

CONSOLE COMPUTER:
System architecture and operating system must be based on latest technologies.
Multi-tasking and parallel processing CPU system, 64bit CPU, 2.2GHz or better.
At least 2TB of storage space or more for 500,000 or more image storage or as per
manufacturer..
Ram: 32 GB or more
Real time spiral/helical reconstruction of 20-images per second with iterative dose
reduction applied.
Medical Grade Console monitor color 21” or more LCD/LED screen with 1920x1200
resolution or better.
Iterative dose reduction technology.
DVD / CDR.
CT control box and console table.
512x512 / 1024x1024 image reconstruction matrix or better.

 MULTI-MODALITY WORKSTATION (2NOs. REQUIRED) should be OEM.


Should be supplied directly from the manufacturer of CT scanner and should not be
supplied locally from the client.
High-speed link to operator console on DICOM Network.
System architecture and operating system must be based on latest dual Xeon processor or
better.
Should have Hi-Resolution Medical Grade LCD/LED screen of 19 inch or more.
CD / DVD writer.
DICOM viewer for viewing ct.
Laser black & white printer capable of printing on multi size papers, 1200dpi or better.
Application software for Workstation given below.

SOFTWARE (INCLUDED AS STANDARD):


Full color volume rendering 3D at console and workstation.
Isotropic volume acquisition at console.
CT Angio at console.
Vessel stenosis analysis at workstation.
3D surface rendering at both console and workstation.
Multi-planar reconstruction at console.
Curved planer reformation at console and workstation.
Contrast media based synchronizing software at console.
ECG gated scan system ECG triggered, and ECG gated cardiovascular examinations and
artifact- free high resolution imaging as standard (retrospective and prospective).
Automatic control of tube current over high and low attenuation areas of patient dose
reduction software for low dose to patient original / certified.
Iterative dose reduction software should be applicable for whole body organ.
Virtual endoscopy / colonoscopy / Bronchoscopy at workstation.
Cerebral blood flow / head perfusion at console and analysis at workstation.
Body blood flow / body perfusion at workstation.
CT DSA subtraction.
Lung volume analysis software on workstation.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

Lung Nodule Analysis software on console.


3D direct lung subtraction software for visualizing lung perfusion defects using contrast
images at console or as per manufacturer.
Single energy metal artifact reduction function.
Complete coronary calcification scanning package including coronary scanning and calcium
scoring software as standard.
Advanced complete cardiac scanning package including complete comprehensive vessel
visualization, automated Stenosis calculation, measurement of ejection fraction, stroke
volume, cardiac output, LV mass and wall thickness, able to demonstrate ventricular wall
motions on color coded map, cardiac reporting program.
Dedicated motion free Coronary CT with intelligent-based automatic phase selection of
cardiac cycle or as per manufacturer..
80kV scan mode for lower radiation dose and pediatric scanning.

DICOM 3.0:
Complete Dicom-3 solution for send, receive, archive, retrieve and print etc. or better.

ACCESSORIES:
200KVA Generator (Optional)
DICOM compatibility dry laser imager for film size 14” x 17” including 500 films.
160KVA online sine wave ups for whole system with a minimum backup of 20 minutes on
full load or equivalent
Dual head programmable, power injector with flow/volume control for both head
independently, mounted on mobile base or ceiling suspended or equivalent.
Standard set of phantoms for calibration of ct.
Table accessories: table pad, arm rest, patient restraint kit, IV pole, infant cradle, flat head
holder, head side pad, u-shaped head pad, head support for coronal scanning, knee cushion.
Accessory rack or cabinet.
Integrated patient vital sign monitor for ECG gated scanning. Should have provision of
displaying ECG signal on display of gantry and on console computer.

INSTALLATION:
Complete Installation of CT.
Lead lining of the CT room (where required) will be done by the vendor who will be
responsible for complete interference free installation from its surroundings to ensure
artifact free examination.
Lead glass for control room 2x3 feet 0.5 mm PB. Equivalent
NOTE:
 The system should be FDA/CE/JIS/MHLW or equivalent approved. 02 certificates
mandatory.
 05 years with parts and services comprehensive warranty.
 Site preparation will be done by the selected bidder.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PNRA Registration will be responsibility of the supplier.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

1.3 DR Machine DIGITAL / FlOOR MOUNTED 550mA XRAY MACHINE


Clinical Specialty Radiology
Generic Name Digital Radiography Machine
Clinical Purpose Digital Radiography Machine is used to detect bone and joint problems, like
complex bone fractures etc.
S.NO. TECHNICAL SPECIFICATIONS
X-RAY GENERATOR:
High frequency inverter type microprocessor x-ray generator.
Three phase 50 kW Generator or better.
Automatic line compensation.
Over load tube protection.
Radiographic kVp 40~150kV or better
Radiographic mA 10~550mA or more
Exposure time: 1ms ~ 6s or better
500 or more Anatomical program
X-RAY TUBE:
Maximum Tension, 150 kVp or better.
Small focus 0.6 mm or better.
Large focus 1.2 mm or better.
Anode Heat capacity 300 KHU or more
FOUR WAY FLOATING TOP TABLE:
Electromagnetic brakes
Longitudinal travel of table top: 900mm or more Lateral/transfer travel of table top:
220mm or more.
Longitudinal travel of bucky: 510mm or more
Moving grid
Grid ratio 40 l/sec, 12:1 as per manufacturer.
FLOOR MOUNTED TUBE COLUMN STAND:
Tube support balancing System with counterweights and Electromagnetic brakes.
Control panel with push button to control vertical travel.
Rotation of tube – collimator assembly +/-90°
Vertical travel: 400-1900mm or better
MANUAL COLLIMATOR
Multi leaf Manual collimator.
LED light indicator for alignment with bucky.
WALL CHEST BUCKY STAND
Chest bucky stand with the cassettes formats maximum up to 35x43cm
Vertical travel 1500mm or better.
Moving grid: 12:1 ratio.
FLAT PANEL DIGITAL X-RAY DETECTOR (FPD) (2NOS)
17x17” Cesium Iodide (Csl) with Amorphous Silicon or better
Pixel Matrix: 3000 (H) × 3000 (V) or better
Pixel Pitch: 150μm or less
DQE: > 70 % or better
A/D Conversion: 14 bit or better

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CONSOLE WORKSTATION (1 NOS.)


Processor : Intel Core I3- or better
Memory : 8GB or better
Hard Drive : 500GB or better
Complete with hardware such as mouse, keyboard etc.
TFT Color monitor 21” or more with Resolution 1280 x 1024 Pixel
DICOM Compliant DICOM 3.0
DICOM 3 CAPABILITY:
Full Dicom-3 capability to send, receive, archive, retrieve and print to be given as standard.
ACQUISITION SOFTWARE:
Operation software for generator and digital panel
Generator synchronization
Image processing
Image management (PACS, HIS/RIS, etc.)
full DICOM 3.0 Compatibility
DICOM worklist from HIS/RIS Store Images through PACS network system
DICOM image print
DICOM MPPS
DICOM CD/DVD
Image quality control tools with pixel fixing tools
AEC and APR
Image cropping, Image mirror, rotate etc
RADIATION PROTECTION:
Imported Protection devices (lead aprons 04 with handers, lead gloves 04 pairs, 0.5mm Pb
equivalent light weight)
Lead glass for control room 1x1 feet 0.5 mm PB. Equivalent.
Lead lining of doors and walls as per requirement for X-Ray Machine / PNRA will be
responsibility of the vendor
INSTALLATION:
Complete Installation of X-Ray Machine will be by trained and authorized engineers.
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.One Certificate should be
mandatory.
 X-Ray Tube, Detector, Work Station and Generator must be from Original
Equipment Manufacturer (OEM).
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PNRA Registration is responsibility of supplier.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

1.4 Doppler Ultrasound Machine


Clinical Specialty Radiology
Generic Name Ultrasound Machine
Clinical Purpose Doppler Ultrasound Machine works on the principles of high frequency sound
waves transmits sound waves through the probe to the body and then
receives it back as echo from internal organs of the body.
TECHNICAL SPECIFICATIONS
Fully Digital Beam Former Having 5 million or More Digital Processing Channels with
Integrated Data Management System Having 1TB Hard Disk Drive for Still and Cine Clips
Storage and 128GB or more SSD for operating system and application software.
Modes
2D/M-Mode, Doppler, Pw, Hprf Doppler, Color Flow Imaging
System Capability 1.5 – 18 MHz or More
Tissue Harmonic Imaging
Viewing Depth: 40cms or better.
Frame Rate: 1500 FPS or better in B-Mode.
Built-In Cine Loop: 50,000 Frames or better oras per manufacturer.
Real time freeze & image magnification ability 10 x pre & post processing
Sweep Speed: Slow, Medium, Fast
12” or better touch command screen for easy operation of the system.
System dynamic range: 50 to 220db or better

Doppler Mode Specifications:


Pulse Repetition Frequency Range; PWD: 1.0 To 22 KHz
Doppler Beam Steering
On Line 4-Ports or more for Trans-thoracic Probes
Doppler Beam Steering and Bi-Directional Stereo Audio
Color Doppler
PW doppler must be continuously steerable in color blood flow imaging mode in real time.
Colorized Spectrum Display
Tissue Harmonic Imaging with Two Frequencies
Elastography
2D Image with Color Flow
Power Doppler
Standard Features
Needle enhancement for biopsy needle visualization
Auto image optimization / quick scan imaging for automatic stc/gain and doppler spectrum
adjustment with optimal image quality by using one touch operation.
B-flow/dynamic flow imaging / e-flow/ glazing flow
Trapezoid imaging/virtual convex imaging with linear probe
Compound/x view+/aplipure imaging for both frequency compounding and spatial
compounding in b/w mode
N-sight / adaptive suppression / precision imaging / xflow/ cross beam to enhance b-mode
imaging, detailed in layers and boundaries and sharpened outlines of the lesions and
reduce cluttering.
3D imaging for the acquisition of volume data and display of 3D images without using a 4D
transducer.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

Live strain rate Elastography with quantification for body organs specially breast to
visualize lesions.
Live Shear wave Elastography with quantification for liver with convex & linear probes to
visualize tissue stiffness by generating images through shear wave propagation, speed, and
elasticity modes.
Measurement Package:
To provide comprehensive software package for measurement of distance circumference,
area, time, depth etc.
System Complete with Following Facilities and Accessories:
21-Inches or better color monitor
Standard Probes:
2.0 – 5.0 MHz or More Multi-Frequency Convex Probe
4.0 – 10 MHz or More Multi-Frequency Linear Probe
4.0 – 10 MHz or More Multi-Frequency TVS Probe
5 – 15 MHz High Frequency Linear
STD Recording Devices:
Built-In CD/DVD Recorder for Digital Image Storage
Built-In / Separate Compatible Imported Online Ups (Minimum Backup Time > 10Minutes)
B/W Thermal Printer. (Model/ Make must be mentioned)
3KVA Online UPS (Optional)
NOTE:
 Probes frequency may vary from manufacturer to manufacturer but shall not down
grade the specs nor effect patient care.
 The system should be FDA/CE/JIS/MHLW. 02 certificates mandatory.
 03 years with parts, probes was added and services comprehensive warranty..
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.

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1.5: DIGITAL MOBILE X-RAY MACHINE WITH BATTERY BACKUP E


Clinical Specialty Radiology
Generic Name Mobile X-Ray Machine
Clinical Purpose Mobile X-Ray can be used to detect bone and joint problems, like complex bone
fractures etc. and easy to move from one place to another place.
S.NO. TECHNICAL SPECIFICATIONS
1
1. GENERATOR
 The highest high-frequency high-voltage generator 20KHz or better
 High control precision, KV, mA real-time control.
 Protection circuit to control the generator temperature, overheating, overcurrent,
overvoltage, tube overload protection
 Generator with wide working voltage range
 Power: 30KW or better
 Tube Current: 10mA~400mA or better
 mAs: 0.1~300mAs or better
 Exposure time: 1ms~8 sec or better
 Exposure voltage kV: 40-150kV or better
 APR: 1000 or as per manufacturer Power Input: 100V-240 AC Single phase, 50/60Hz

2. X-RAY TUBE
 Rotating anode X-ray tube
 Anode heat storage capacity 140kHU or better
 Focal spot: dual focus 0.6 mm/1.2 mm or better
 Tube Voltage: 40~ 150kV or better
 Inherent filtration: 0.9mmAl or better

3. FLAT PANEL DETECTOR


 Portable wireless flat panel detector that make examination easier even on a stretcher bed
or wheelchair.
 Amorphous silicon (a-Si) semiconductor with cesium lodide (CsI) scintillator
 DQE: 70% or better
 Pixel area(Detector size): 14x17inch or better
 Pixel size: 140 μm or better
 Matrix size: 2560×3072 or better
 Dynamic range: 16bit or better
 Spatial Resolution: 3.6lp/mm or better
 Imaging time of imaging system: 6 sec or better
 Preview time of imaging system: 5 sec or better
 Data transmission method: Ethernet
 Auto charging inside the detector storage facility should be available
 Electronic detector lock

4. Movements
 Tube assembly vertical plane rotation angle: -90°~90° or better

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 Tube assembly horizontal axis rotation angle: -90°~90° or better


 Tube assembly tilting angle: -30°~90° or better

5. BATTERY BACKUP
 Battery backup of 100 exposures and can drive 50 KM was changed to 5Km routine
usage when fully charged.
 Charging time: 3.5h or better
 The sensor in the front to automatically stops the device if a slight pressure is detected
 Dual way braking
 Unit movement driven by power or manual

6. ACQUISITION WORKSTATION
 Workstation as per manufacturer
 CD/DVD R/W
 Image acquisition workstation monitor: LCD Screen size: 17 inch or better
 Image processing system meets the DICOM 3.0 achieving management over patients and
images.

NOTE:
 The system should be FDA/CE/JIS/MHLW or equivalent approved. 01 certificate
mandatory
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in
case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PNRA Registration is the responsibility of supplier.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

1.6 SINGLE PLANE CARDIAC ANGIOGRAPHY MACHINE


Clinical
Radiology
Specialty
Generic
Interventional Radiology
Name
Clinical Angiography or arteriography is an imaging technique used in medicine to visualize the
Purpose inside, or lumen, of blood vessels and organs of the body, such as the arteries, veins, and
heart chambers.

TECHNICAL SPECIFICATIONS
A fully digital flat panel single plane IR Angiography system, dedicated for diagnostic &
interventional Radiology examinations. Head to toe patient coverage without patient re-
positioning should be possible. The Angiography system should comprise of the
following Configuration:
POSITIONING ARM:
STAND:
Ceiling mounted stand with manual / motorized movements, providing free access to
patient table from all 3x sides
Real time display of rotation angulations.
Geometry: C-arm / G-arm
C arm depth of 86cm or more
RAO / LAO +/- 120 ° or more
C-arm permits 90° cranial and 90° caudal angulation of the imaging system
3D Rotational angiography with a speed of up to 50°/sec or more. It should be possible
to achieve rotational scan with C-arm positioned at head end or nurse end as per user
preference and clinical requirement
Isocentric Height: Variable / Fixed. Variable / Fixed. Focus spot to iso-center should be
75 cm or more
Auto Positioning: Programmable auto positioning of selected angulations. (50 or more
programmable positions.). Ability to recall stand position by reference image should be
possible.
The control panel can be mounted at any side of the patient table.
All the rotational / angles should be available and digitally displayed in the control and
examination room.
Motorized / manual parking of the positioning arm should be possible
DIGITAL FLAT PANEL:
Image matrix of 2480 x 1920 x 16 bits or more. Systems with higher matrix will be
preferred
30 x 40cm or more sized detector with five formats or more
Built in temperature stabilizer preferably without chiller
Digital flat panel detector with pixel pitch of 160 micron or less and DQE of 75% at 0
lp/mm
Integrated no touch collision protection feature or as per manufacturer.
All other standard accessories according to this digital flat panel.
Removable Antiscatter grid for lowering dose to infants & paeds

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PATIENT SUPPORT/ TABLE:


Interventional Table:
Floor mounted with up down / vertical, longitudinal table top length of minimum 315
cm or more
Longitudinal travel.: 110 cm or more
Lateral Travel + - 15 cm or more
Table Tilting should be provided
CPR: with tabletop In any table longitudinal position, without the need of retraction
Table side movement controls with one additional control to control the movements
from any side of the table.
Table top should be of such construction in material and durability to accept patients
weight of not less than 220 kg or more
Table top should have metal free over hang for un-obstructed imaging coverage & having
integrated hemodynamic monitoring system controls
Complete accessories should be provided including arm holder, hand grip, arm support
and arm rest and positioning aids.
Pivot +/- 90Deg or better
X-RAY GENERATOR:
Microprocessor based high frequency using fiber optic for data communication between
each imaging system.
Dedicated X-Ray generator of 100 kW.
Radiographic rating minimum 1000 mA at 100KV
Serial filming exposures, Auto exposure optimization with shortest exposure of 1ms,
with automatic kV and mA control for optimum image quality.
The system should have capability of digital radiography and fluoroscopy.
Should have capability of doing digital pulsed fluoroscopy at at 3.75/7.5/ 15 / 30 pulses
per second. Automatic kV, mA & pulse width regulation facility.
DIGITAL IMAGING AND ACQUISITION / FLUOROSCOPY.
DIGITAL SYSTEM:
Pulse Fluoroscopy at 30/25 FPS, 15/12.5 FPS, 7.5/6 FPS or better with 2k x 2k resolution
Parallel processing capability / multitasking facility.
Real time filtering and road map function.
Default storage of the last 20sec, programmable up to 999 images or more of fluoroscopy
for reference or archiving
Cine Acquisition at 3.75, 7.5, 15 and 30 pulses per seconds
Storage capacity 50,000 images or more in 1024x1024 matrix
Integrated dose monitoring and dose structured reporting in DiCOM.
X-RAY TUBE:
Dual focal with at least 5 MHU or better anode heat storage capacity with anode heat
dissipation rate of 10,000W or more to enable continuous heat dissipation during serial
exposure.
Dual/Triple focus, rotating anode. Focal spot sizes 0.2/0.5, and 1.0 mm or better:
Dose management with fluoro Cu filters. : Copper filters: 0.2, 0.5, and 1.0 mm CU
equivalent
Anode cooling rate 1500 KHU/min or more

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MONITORS:
Flat Screen 19” TFT of 1024 x 1024 matrix supplied in control room.
Monitors should be ceiling mounted in the operation room.
One 54" or better 8MP medical grade monitor with integrated tableside control in touch
panel in operation room also the screen should have at-least 6 different layout to
incorporate all applications. (must be from the same OEM)
All black & white monitors will be of Medical Grade, complied with international
standards for medical monitors.
CONTROLS:
All controls of digital imaging system, incl. Post Processing & Quantification analysis shall
be in the control room while replay / display of reference image should be available in
the examination room. Wireless remote control for playback and processing functions in
the examination room. Table side control through touch panel at the table side should be
available.
Table side controls are essential. Controls should be manageable from both sides of the
table. Wireless foot paddle should be offered as standard having at least 3 paddles (user
configurable), based on battery with minimum duration of 7 days/charge
RECORDING / ARCHIVING & COMMUNICATION SYSTEM:
Recording / archiving system should be DICOM-3 compatible.
DICOM (send/storage, commitment, retrieve/query)
Ethernet connection to connect with other terminals.
Integrated Intercom system.
DICOM-3 Compatible.
Edge enhancement, adjustable view speeds & post processing, Offline QVA
Quantifications on Workstation should be offered as standard
High resolution 19” TFT Monitor.
CD/DVD writer and CD/DVD ROM drive.
The bidders should quote their own licensed software.
SOFTWARE / HARDWARE PACKAGES:
Standard Quantification packages vascular quantitative analysis including vessel
analysis, vessel size and stenosis assessment
Automatic loop replay after acquisition or fluoroscopy
Rotational angiography software 3D visualization of vascular
pathologies from a single rotational angiographic X-ray acquisition
CT-like imaging to visualize bone, soft tissue, and vessels
Automatic loop replay after acquisition or fluoroscopy.
Dynamic real time pan / zoom.
DSA
Dual Phase acquisition and Dual View functionality which should allow simultaneous
visualization of two 3D data sets. The System should have Open Trajectory feature helps
visualize the peripheral part of the liver, while the 3D imaging technology should allow
for simultaneous multiple lesion segmentation.
All controls of digital imaging system incl. Post-processing & Quantification shall be in
the examination as well as control room.
Single axis rotation
All the advance clinical packages offered by the vendor should be from the OEM of the
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angio system
Software with ablation feature provides a comprehensive solution for treatment
planning and live needle guidance during interventional
ablation procedures.
The workflow-based tool to guide detection and treatment of tumors and feeder vessels
to multiple lesions. Based on a segmented 3D volume, the software should automatically
analysis the vasculature of lesions and provides suggestions about feeder vessels to the
segmented lesions. having facility of EP Studies and also integration with IVUS, iFFR and
FFR must be provided
RADIATION PROTECTION:
Ceiling suspended tilt able lead glass for radiation protection of operators head / neck
regions.
Collision tolerant.
Lower body radiation protection flaps.
PHYSIOLOGICAL HAEMODYNAMIC MONITORING SYSTEM:
should be for paeds and adults having control on same touch screen which also controls
all other functionality
Multichannel to record at least 2 channels IBP, Cardiac output with thermo dilution
method, Surface ECG in any configuration and simultaneous 12 lead ECG, NIBP and SpO2
measurement.
Digital display of all the parameters like IBP, Heart rate, cardiac output parameter.
It should be possible to store the waveforms on the hard disk of the physiological
recording system.
The hemodynamic monitoring system should include following accessories :
2x invasive blood pressure reusable transducer.
Reusable interface for 12 lead ECG (2 Nos)
NIBP cuffs (02 Nos)
Holder for mounting the IBP transducer alongside the patient table.
Upgradable to EP System.
Angio Compatible UPS with standard backup time of 20 mints was changed to 160mins.
200KVA Generator to be quoted as optional.
ACCESSORIES:
Online UPS of 160KVA
Single head Power Injector with disposable syringes 500
Wall mounted / trolley mounted hangers for lead aprons
Thyroid Collars with gonadal shields 10 x
Lead glass 5 x 2 ft
Knee pads
Complete building/civil work for state of the art Angio suite including storage aluminum
racks, aluminum doors with elbow action controls, paneling, lead lining , flooring , paints
etc.
Oxygen and suction system connection with the existing hospital pipeline.
Split air conditioner units for whole suite.
Complete electricity works from power station to Anglo room including earthling, power
Racks, breakers, DB etc. Lead lining of walls, windows and doors complete full length
NOTE:
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The system should be FDA/CE/JIS/MHLW or equivalent approved and 02 certificates are


required mandatory.
 Gray structure will be provided by HMC whereas the renovation of site will be
the responsibility of the firm.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the
supplier in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of
the equipment.
 PNRA Registration will be responsibility of the supplier/firm.

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1.7 COLOR DOPPLER TRUS (TRANS-RECTAL PROBE)


Clinical
Urology, Radiology
Specialty
Generic
Trans Rectal Ultrasound Machine
Name
Clinical In TRUS, sound waves are bounced off internal tissues or organs and make echoes. The echoes
Purpose form a picture of body tissue called a sonogram. Transrectal ultrasound is used to look for
abnormalities in the rectum and nearby structures, including the prostate. Also called endorectal
ultrasound, ERUS, and TRUS.

TECHNICAL SPECIFICATIONS
 System must have 300, 000 or more Digital Processing Channels
 Integrated Data Management System having 500 GB or more Hard Disk Drive for still and
cine Clips storage
 Should have System Capacity of 1.5-16 MHz or More
 Must have 4 Active Probe Connectors
 Should have Tissue Harmonic Imaging
 Should have Maximum Viewing Depth of 35 cm or more
 Must have Frame Rate 1000 FPS or more
 Should have Pre and Post Processing option with Raw Data Storage
 Must have user-defined programmable keys for custom selection by the User
 Sweep Speed: Slow, Medium, Fast
 Should have Full Screen Zoom Capability
 Must have 10" or more angle adjustable secondary Touch Screen for easy operation of the
system
 System Dynamic Range: 200 dB or More
 Must have 5 or more USB 3.0 Ports
 Must have VGA and HDMI Port to connect system with Multi-Media/ Projector

Color Doppler
 Colorized Spectrum Display
 Tissue Harmonic Imaging with 3 or more harmonic frequencies
 2D Image with Color Flow
 Power Doppler/ Directional Power Doppler Imaging
 Auto Image Optimization/quick scan for single button optimization of all scanning
parameters
 Including 8-Segment STC/ TGC plus overall gain
 Sonoct/compound/aplipure imaging for both frequency compounding and spatial
compounding in B/W and color Doppler
 Wide View/Trapzoid Imaging for Linear Probe
 Doppler Sensitive Imaging for Low Flow Velocity Vessels SMI/ B-Flow/ HR Flow or
equivalent
 Auto IMT calculation in Carotid with Linear Probe
 Adaptive Suppression imaging/precision imaging to enhance b-mode imaging detailed in
layers and boundaries and sharpened outlines of the lesions and reduces cluttering
 Doppler Beam Steering and Bi-Directional Stereo Audio

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System complete with following facilities and accessories


 19-inches or more color monitor with resolution 1280*1024 or better
 1.5-6 MHz multi-frequency convex probe for B/M/CDI/PW (Probe Model and Frequency
Range should be mentioned)
 3-12 MHz Multi-Frequency Linear Probe for B/M/CDI/PW (Probe Model and Frequency
Range should be mentioned)
 3-12 MHz Multi-Frequency Trans Rectal Probe having Radius of 8 mm or more or biplane
for Prostate (Urology) (Probe Model and Frequency Range should be mentioned)
 5- 16 MHz or better Multi-function Linear Probe (Probe Model and Frequency Range
should be mentioned)
 Needle Tracking/ Visualization with Biopsy Kit.
 Built-In CD/DVD recorder for Digital Image Storage
 B/W Thermal Printer
 System should have DICOM compatibility
 Online UPS for Whole System (3KVA)

NOTE:
 The system should be FDA/CE/JIS/MHLW approved 02 certificates are required
mandatory.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in
case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with
the supply of equipment, which will include calibration and validation of the
equipment.

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S. NO. 2 (MODULAR OT’S)


2.1
INTIGRATED MODULAR OPERATING ROOM BOQ
SR. NO. PARTICULARS UOM QTY
1 MODULAR WALL PANEL SYSTEM:
a MODULAR WALL PANEL SYSTEM: STAINLESS STEEL POWDER Sq.m 1
COATED WALL PANELS FOR OPERATION ROOM.

b DECORATIVE GLASS WALL PANELS FOR OPERATION Sq.m 1


THEATERS: 1 GLASS WALL PANELS FOR EACH OPERATION ROOM

c MODULAR WALL PANEL SYSTEM: GALVANIZED STEEL POWDER Sq.m 1


COATED WALL PANELS FOR CLEAN CORRIDOR (AS PER SITE
REQUIRMENTS)
2 CLEAN CEILING SYSTEM: -
a CEILING SYSTEM: CLEAN ROOM METAL CEILING SYSTEM FOR Sq.m 1
OPERATION THEATERS
b CEILING SYSTEM: CLEAN ROOM METAL CEILING SYSTEM FOR Sq.m 1
CLEAN CORRIDOR. (AS PER SITE REQUIRMENTS)
3 X‐RAY VIEWER: 3 FILM LED X‐RAY VIEWER FOR OPERATING Each 1
ROOM
4 PERIPHERAL LIGHTS: CLEAN ROOM PERIPHERAL LIGHTS FOR Each 1
OPERATION ROOM.
5 DOOR SYSTEMS: -
a DOOR SYSTEM: AUTOMATIC SINGLE WING SLIDING DOOR FOR Each 1
OPERATION THEATER | 1500 X 2100 MM OR AS PER SITE REQUIR.

b DOOR SYSTEM: AUTOMATIC DOUBLE WING SLIDING DOOR FOR Each 1


CLEAN CORRIDOR | AS PER SITE REQUIR.
C DOOR SYSTEM: Automatic SINGLE LEAF HINGED DOOR | 1050 X
2100 MM FOR DIRTY CORRIDOR
d DOOR SYSTEM: MANUAL SINGLE LEAF HINGED DOOR | 1050 X Each 1
2100 MM FOR DIRTY CORRIDOR
6 CLEAN ROOM FLOORING: -
a CLEAN ROOM FLOORING: STATIC DISSIPATIVE HOMOGENOUS Sq.m 1
VINYL FLOORING FOR OPERATION THEATERS

b CLEAN ROOM FLOORING: HYGIENIC VINYL FLOORING FOR Sq.m 1


CORRIDOR, etc.
7 CABINET SYSTEM: STAINLESS STEEL MEDICAL CABINET FOR Each 1
STORAGE IN EACH OR
8 OR CONTROL PANEL: DIGITAL SURGEON CONTROL PANEL WITH Each 1
TOUCH SCREEN FOR EACH OR
9 PENDANT SYSTEM: DUAL ARM SURGICAL PENDANT Each 1
10.a PENDANT SYSTEM: SINGLE ARM ANESTHESIA PENDANT Each 1

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10.a PENDANT SYSTEM: DOUBLE ARM ANESTHESIA PENDANT Each 1


11 OPERATING LIGHT SYSTEM: DOUBLE DOME LED OPERATING Each 1
LIGHT WITH CAMERA & HD MONITOR ON 3RD ARM

12.1 ROUND/SQUARE LAMINAR AIR FLOW CEILING 3000MM or Each 1


MORE FOR CIRCULAR LAF / 3200MM x 3200MM or MORE FOR
SQUARE LAF
(LAF CEILING PRIMING ILLUMINATION)
12.2 FLUFF SEPARATORS FOR RETURN AIR NEAR CEILING Type A 670 x Each 1 SET
370 mm OR BETTER - Return Air Grill (4 PER OR)
13 DEDICATED HYGENIC AIR HANDLING UNITS (Euro vent/ Cetiat Each 1
/ Equivalent certified).
14 AUTOMATIC WATER DISPENSER FOR SCRUB AREA Each 1

15 4K VIDEO MANAGEMENT & DOCUMENTATION SYSTEM: AUDIO Each 1


VIDEO MANAGEMENT, DOCUMENTATION & COMMUNICATION (2
WAY AUDIO AND 1 WAY VIDEO)

16 FILTERSEPT 7 OR 10: HEPA FILTER CEILING DIFFUSERS WITH Each 1


HEPA FILTERS FOR CLEAN CORRIDOR
LOCAL WORKS TO BE EXECUTED WITH PROCUREMENT OF MODULAR OPERATION THEATERS
17 HVAC DUCTING WORKS COMPLETE IN ALL ASPECTS SqFt. 1
18 AUTOMATIC CONTROL SYSTEM Job 1
19 FOUNDATION PAD FOR HVAC EQUIPMNT (Civil Works) SqFt. 1

20 ELECTRICAL WORKS Sq.Ft. 1


21 INSTRUMENT AND GUAGES Each 1-SET
22 ALUMINUM WASHABLE FILTER FOR FRESH AIR Each 1

MODULAR OPERATION THEATER


1 WALL PANEL SYSTEM
a STAINLESS STEEL POWDER COATED WALL PANELS FOR OPERATION Sqm.
THEATERS
General Description of Wall Panel System ‐ The Wall panel system is manufactured in
multilayer technology. From the front side, metal sheets are bent at the right angle
backwards at the top and bottom of the panel.
Panel construction allows easy assembling / dismantling of single panel to make changes /
modifications of installation on the back of wall panel giving seamless finish.
 Wall panels are made of stainless steel, powder coated in any RAL color with antimicrobial
properties added to the coating during production process.
 Cladding panels must be connected to the substructure “screw-less”. Panels must be single
piece “floor ceiling height” – No horizontal joints are allowed.
 Horizontally/Vertical wall panels are joined tight thanks to specifically shaped edge.
 The removable silicone seal is resistant to UV, detergents, bactericidal products, water,

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steam and chemicals used to sterilize Operation Theater complying with the requirements
of norm as per manufacturer.
Material ‐ Stainless Steel / thickness of metal sheet of min. 8 mm or better.
Finish: Powder Coated in any RAL Color with antimicrobial protection.
Joints ‐ The wall panels are fixed on the sub‐structure leaving 4-6mm intermediate space
between the panels and is filled / covered by removable hermetic silicon seal / gasket. The
removable silicon seal is resistant to UV, detergents, bactericidal products, water, steam and
chemicals used to sterilize Operation Theater.
Corners ‐ Wall to wall and wall to ceiling connections are coved/diagonal made of stainless
steel sheet powder coated finishing like the wall panels and smoothly integrated with the
wall panels on the sub‐structure assembled similar like wall panels with screws covered with
removable silicone gasket.
Sub‐Structure Profiles ‐ Floor rails are made of galvanized steel sheet of appropriate
thickness with base height 80-100mm fastened with screws and dowels over leveled screed.
The sectional supports are suitable to support to the wall panels, profile length shall be
adjusted on site according to the available height. U‐profiles are used for connection to wall
panels and existing building walls.
The sub‐structure is fastened with concrete elements of the building.

b DECORATIVE GLASS WALL PANELS FOR OPERATION THEATERS: Sqm


1 GLASS WALL PANELS FOR EACH OPERATION ROOM WITH HIGH DEFINITION
PICTURE
DECORATIVE GLASS WALL PANELS FOR OPERATION THEATERS WITH SUB-
STRUCTURE
 The glazed modules should made up of bearing frame made of extruded aluminium
profiles (painted with polyester paint or anodized) with a safety glass 6-10 mm thick
layered with 0.38 polished PVB (POLYVINIL BUTYRAL) (available color should mention
for selection).
 The frames should be hooked on the structural corner posts through the same rack
connection of the blind panels and should be perfectly leveled for the insertion of
directable slat blinds, decorative films for a better harmonization of settings with
chromatic effects.
 The glazed modules are made up of a honeycomb aluminum back panel 10mm where a
safety glass 5mm thick is applied as per manufacturer.
c GALVANIZED STEEL POWDER COATED WALL PANELS FOR CLEAN CORRIDOR Sqm.
General Description of Wall Panel System ‐ The Wall panel system is manufactured in
multilayer technology. From the front side, metal sheets are bent at the right angle
backwards at the top and bottom of the panel.
Panel construction allows easy assembling / dismantling of single panel to make changes /
modifications of installation on the back of wall panel giving seamless finish.
 Wall panels are made of galvanized steel, powder coated in any RAL color with
antimicrobial properties added to the coating during production process.
 Gaps between panels (approx. 6 mm) are filled with removable pushed‐in silicone hermetic
seal.
 Horizontally /Vertical wall panels are joined tight thanks to specifically shaped edge.
 The removable silicone seal is resistant to UV, detergents, bactericidal products, water,
steam and chemicals used to sterilize Operation Theater complying with the requirements
of norm as per manufacturer.
Material ‐ Stainless Steel / thickness of metal sheet of min. 8 mm or better.

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Finish: Powder Coated in any RAL Color with antimicrobial protection.


Joints ‐ The wall panels are fixed on the sub‐structure leaving 4-6mm intermediate space
between the panels and is filled / covered by removable hermetic silicon seal / gasket. The
removable silicon seal is resistant to UV, detergents, bactericidal products, water, steam and
chemicals used to sterilize Operation Theater.
Corners ‐ Wall to wall and wall to ceiling connections are coved/Diaganol made of stainless
steel sheet powder coated finishing like the wall panels and smoothly integrated with the
wall panels on the sub‐structure assembled similar like wall panels with screws covered with
removable silicone gasket.
Sub‐Structure Profiles ‐ Floor rails are made of galvanized steel sheet of appropriate
thickness with base height 80-100mm fastened with screws and dowels over leveled screed.
The sectional supports are suitable to support to the wall panels, profile length shall be
adjusted on site according to the available height. U‐profiles are used for connection to wall
panels and existing building walls.
The sub‐structure is fastened with concrete elements of the building.
2 CLEAN ROOM METAL CEILING SYSTEM FOR OR’s & CORRIDOR Sqm.
General Description: False ceiling system made up of metal tiles installed with hidden
structure. Conceived to reduce the air exchange between the plenum and the environment,
making the false ceiling suitable for use in hospitals and pharmaceutical environments.
Construction– The clean room suspended ceiling system is made of specified material
having specialized durable powder coating with integrated antimicrobial protection on the
face side in specified color. The ceiling panels have the modular grid size 600 x 600 mm and
the wall to ceiling connection is coved, angular or 90 deg. as per customer choice. The ceiling
panels are "Clip‐in" type and complementary to the wall panel system. The ceiling system
allows smooth integration with Laminar flow ceiling and other fixtures giving hygienic finish
to the operating room. The suspension for "Clip‐in" ceiling panels are made of Galvanized
Steel allowing easy and quick assembling / dis‐assembling for normal operations of
maintenance.
Material – Ceiling panels are made of painted steel sheet 0.5mm thick, powder coated in any
RAL color with antimicrobial properties.
Finish: The ceiling panels are powder coated in RAL color having bactericidal properties.
Substructure: Hidden structure: tubular profiles set in parallel (with the same distance of
tiles) and fixed on main runners in galvanized steel according to required ceiling layout
project requirements. Tiles edges will be properly shaped to be clip in their hidden structure.
Profiles will be installed at a distance of 600 mm between each other. Adjustable suspension
system through hangers with hook spring.
Sealing system: The false ceiling will be completely sealed and will meet the cleanliness
requirements; it will present a compact and uniform result with a perfect separation between
plenum and the environment below.
3 LED X‐RAY FILM VIEWER FOR OPERATING ROOM TRIPLE FOLD Each
4 CLEAN ROOM PERIPHERAL LIGHTS FOR OPERATION THEATERS & CORRIDOR Each
General Description – Luminary designed to modular and plaster‐board suspended ceilings,
equipped with highly efficient LED source. Sheet-steel body powder coated with white (RAL
9003) epoxy powders thermosetting at 180°C, after degreasing, phosphatizing and washing
treatment. The luminaire is equipped with inside gaskets and guarantees the total protection
IP65 against dust and water splashes in the optical hollow. Designed to be used in chemical
laboratories, hospital rooms, operating theatres, clean rooms or anywhere a protection is
needed.
Optical group: MOT high-transmittance opal methacrylate diffuser to ensure an optimal

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lighting diffusion with high uniformity. The diffuser is UV-protected for a better resistance to
weathering.
 Suspended light system to smoothly integrate with modular and plaster‐board
suspended ceilings,
 Luminary body made with steel sheet and powder coated in white.
 Aluminum free frame.
 Hermetic sealed body to prevent foreign bodies when closed
 Resistant to disinfectants and UV radiation with white-coated steel frame
 Lamp: LED
 Power: 50W
 Protection Class: IP65
 Dimension: 600X600mm
 RGB light source to be quoted as optional.

5 DOOR SYSTEMS
a AUTOMATIC SINGLE WING SLIDING DOOR FOR OPERATION THEATER | As Per Each
Site Requirement
Door Wing – Single wing of thickness 40mm with 1.5mm Stainless Steel AISI 304 brushed
finish or powder coated outer skin fully closed construction. Door acoustically and thermally
isolated with highly pressured polyurethane foam of density 50 kg/m3 additionally
strengthening construction of the door wing with silicone gaskets.
Handles – Stainless Steel “C” or as per manufacturer shaped long handles from external side
and recessed type handle from the inner side of the door wing of the door wing.
Door Frame – made of 1.5mm thick Stainless Steel sheet AISI 304 brushed finished or power
coated in any RAL colour. Fabricated in two (2) parts internal and external to smoothly
integrate with the masonry wall and modular wall system.
Inspection Window – 400 x 600 mm double glazed (safety glass) with electronic privacy
having control button provided near the door accessible from inside of the OT.
Safety Sensor – 2 set of photocells in door frame along with infrared sensor at door drive
level on inner and outer side of the door.
Activators – Rubber hit switch/touchless on both sides of the door frame for full opening of
the door. For touchless operation proximity sensors are installed on both side of the door can
be programmed for partial / full opening of the door. Stainless Steel Elevator switch with LED
light Symbol provided inside and outside of the door frame for full open, partial open and
constant opening during cleaning and maintenance. Programmatic switch with key will be
provided on the door drive cover for program selection.
Automatic door Drive –slide away system or any renowned brand as per the
manufacturer’s selection, capable for controlling for full opening, reduced / partial opening,
locking, one‐way, fire alarm integration with battery back‐up module. In case of power
failure the battery back‐up will operate the door however the door can be manually
operated.
Drive Cover – Stainless Steel AISI 304 brushed finished or powder coated in any RAL color.
Door Dimension – 1500 X 2100 MM OR As Per Site Requirements
b AUTOMATIC DOUBLE WING SLIDING DOOR FOR CORRIDOR | As Per Site Each
Requirement
Door Wing –Double wing of thickness 40mm with 1.5mm Stainless Steel AISI 304 brushed
finish or powder coated outer skin fully closed construction. Door acoustically and thermally
isolated with highly pressured polyurethane foam of density 50 kg/m3 additionally
strengthening construction of the door wing with silicone gaskets.

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Handles – Stainless Steel “C” shaped long handles from external side and recessed type
handle from the inner side of the door wing of the door wing.
Door Frame – made of 1.5mm thick Stainless Steel sheet AISI 304 brushed finished or power
coated in any RAL colour. Fabricated in two (2) parts internal and external to smoothly
integrate with the masonry wall and modular wall system.
Inspection Window – 400 x 600 mm double glazed (safety glass) with electronic privacy
having control button provided near the door accessible from inside of the OT.
Safety Sensor – 2 set of photocells in door frame along with infrared sensor at door drive
level on inner and outer side of the door.
Activators – Rubber hit switch/touchless on both sides of the door frame for full opening of
the door. For touchless operation proximity sensors are installed on both side of the door can
be programmed for partial / full opening of the door. Stainless Steel Elevator switch with LED
light Symbol provided inside and outside of the door frame for full open, partial open and
constant opening during cleaning and maintenance. Programmatic switch with key will be
provided on the door drive cover for program selection.
Automatic door Drive BEAM UNSLIDE–slide away system or any renowned brand as per
the manufacturer’s selection, capable for controlling for full opening, reduced / partial
opening, locking, one‐way, fire alarm integration with battery back‐up module. In case of
power failure the battery back‐up will operate the door however the door can be manually
operated.
Drive Cover – Stainless Steel AISI 304 brushed finished or powder coated in any RAL color.
Door Dimension – As Per Site Requirements
c AUTOMATIC SINGLE LEAF HINGED DOOR FOR DIRTY CORRIDOR| As Per Site
Requirement Each
Door Wing – Single wing of thickness 40mm with 1.5mm Stainless Steel AISI 304 brushed
finish or powder coated outer skin fully closed construction. Door acoustically and thermally
isolated with highly pressured polyurethane foam of density 50 kg/m3 additionally
strengthening construction of the door wing with silicone gaskets.
Handles – Stainless Steel “C” shaped long handles from external side and recessed type
handle from the inner side of the door wing of the door wing.
Door Frame – made of 1.5mm thick Stainless Steel sheet AISI 304 brushed finished or power
coated in any RAL colour. Fabricated in two (2) parts internal and external to smoothly
integrate with the masonry wall and modular wall system.
Inspection Window – 400 x 600 mm double glazed (safety glass) with electronic privacy
having control button provided near the door accessible from inside of the OT.
Safety Sensor – 2 set of photocells in door frame along with infrared sensor at door drive
level on inner and outer side of the door.
Activators – Rubber hit switch on both sides of the door frame for full opening of the door.
For touchless operation proximity sensors are installed on both side of the door can be
programmed for partial / full opening of the door. Stainless Steel Elevator switch with LED
light Symbol provided inside and outside of the door frame for full open, partial open and
constant opening during cleaning and maintenance. Programmatic switch with key will be
provided on the door drive cover for program selection.
Automatic door Drive – BESAM UNISLIDE slide away system or any renowned brand as per
the manufacturer’s selection, capable for controlling for full opening, reduced / partial
opening, locking, one‐way, fire alarm integration with battery back‐up module. In case of
power failure the battery back‐up will operate the door however the door can be manually
operated.
Drive Cover – Stainless Steel AISI 304 brushed finished or powder coated in any RAL color.
Door Dimension – As Per Site Requirements

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d. MANUAL SINGLE DOOR FOR DIRTY CORRIDOR| As Per Site Requirement


Door Wing – Single wing of thickness 40mm with 1.5mm Stainless Steel AISI 304 brushed
finish or powder coated outer skin fully closed construction. Door acoustically and thermally
isolated with highly pressured polyurethane foam of density 50 kg/m3 additionally
strengthening construction of the door wing with silicone gaskets.
Handles – Stainless Steel “C” as per manufacturer shaped long handles from external side
and recessed type handle from the inner side of the door wing of the door wing.
Door Frame – made of 1.5mm thick Stainless Steel sheet AISI 304 brushed finished or power
coated in any RAL colour. Fabricated in two (2) parts internal and external to smoothly
integrate with the masonry wall and modular wall system.
Inspection Window – 400 x 600 mm double glazed (safety glass) with electronic privacy
having control button provided near the door accessible from inside of the OT.
Drive Cover – Stainless Steel AISI 304 brushed finished or powder coated in any RAL color.
Door Dimension – 1500 X 2100 MM OR As Per Site Requirements
6 CLEAN ROOM FLORRING:
a STATIC DISSIPATIVE HOMOGENOUS VINYL FLOORING FOR OPERATION Sqm.
THEATERS
General Description ‐ Static dissipative homogenous vinyl flooring of 615mm x 615mm tile
size OR ROLL of 2.0 mm thickness sliced from highly compressed solid block of homogenous
material having conductive chips compressed inside forming a dense network of tiny black
veins giving life‐time or permanent static dissipative functionality to the floor. The flooring
offers an electrical resistance of 106 ≤ R ≤ 108 ohms (IEC 61340‐4‐1 / EN 1081 (100V)
ANSI/ESD 7.1) and the electrostatic discharge is through the whole thickness of the tile via
the conductive veins. The flooring is bacteriostatic in accordance with SNV 195 920, chemical
resistant is excellent in accordance with ISO 26787 / EN 423, slip resistance rating is R9
according to DIN 51130. The floor is installed giving hygienic finishes suitable for operating
rooms with coved edges at the wall connection and factory molded corners, all joints are heat
welded using welding rods of matching color. The vinyl floor is installed on smooth leveled
surfaced prepared by applying necessary primer and self‐leveling compound over the
existing floor using conductive glue / adhesive and copper tape for grounding.

b HOMOGENOUS VINYL FLOORING FOR CORRIDOR Sqm.


General Description ‐
Homogenous vinyl flooring
Minimum thickness of 2.0 mm in Roll
Made with steel-belt press technology to ensure consistent quality.
The supplier should offer choice of colour to the end user choice
Must meet the requirements of EN 14041 for reaction to fire, slip resistance,
Thermal conductivity and Body voltage, Completely heat welded joints of matching color.
7 CABINET SYSTEM: STAINLESS STEEL MEDICAL CABINET FOR STORAGE IN EACH
OR Each
STAINLESS STEEL MEDICAL CABINET FOR STORAGE
 The cabinet body must be stainless steel 304 1 mm thick and self-supporting,
 Smooth body with no edges and welded on all sides and no inside frames and rivets etc.
 Cabinet easy to integrate and completely flushed with wall panel system.
 The cabinet body and doors are flushed with wall panel surface.
 Cabinets are sealed with a hermetic removable silicone seal with antibacterial silver ions
additive
 Double wing Cabinets door with self-closing stainless steel hinges

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 Wide angle opening door to min. 120° or better.


 Doors with Safe Glass, fitting in double steel sheet window frame.
 Doors window with safe glass, min. 6 mm thick, smooth door edges, no rivets, screws, etc.
 Must be zero dirt penetration. Equipped with rubber seals, fixed (pushed in) on the door
wing (using adhesives is not allowed).
 Stainless steel 304, 1mm thick Height adjustments shelves.
 Back wall and shelves shall be supported from bottom by trapeze profile to avoid bulging
of the steel.
 Height adjustable feet to allow for leveling of the cabinet.
 All edges are rounded and safe to prevent bacteria colonies and easy cleaning.
 External Dimensions – 1200 x 450 x 2100 mm or as per site requirement
8 SURGEON CONTROL PANEL WITH TOUCH SCREEN Each
The Digital Operation Theater Control Panel consists of 21” multifunction control touch
screen with a resolution min. 1024 x 768, is designed to ensure efficient work of medical
personnel in the maximum comfort. The system allows to control below mentioned
equipment in the operating room.
 Digital Real Time & Date
 Elapsed Timer
 Peripheral Light Control
 Door access
 Atmosphere (Temperature and humidity display and control through HVAC)
 Temperature and Humidity control of HVAC system
 Temperature and humidity Run time display
 HVAC filter and HEPA Filter status
9 DOUBLE ARM SURGICAL PENDANT Each
General Description - Ceiling mounted Surgical Pendant system, powder coated,
hygienically smooth surface, impact and disinfectant resistant. Extension arms shall be made
from extruded aluminum section with specially formed five chamber system for extremely
high torsional strength. The pendant system shall have the flexibility to retrofit or exchange
medical gas outlets and electrical installations easily, without any need to demount the
suspension arm and service heads. Ceiling mounted supply unit consist of suspension arms,
service head and ceiling mounted components.
• Shelves – 2 Pcs
• Drawer – 1 Pcs
• No. of Arms: 2
• Length of first arm: 800/ 1000mm
• Max. degree of rotation at each arm: 330-350°
• Max. Loading capacity: 200 Kg
• Braking system: Electromagnetic/ Pneumatic brakes to control horizontal movement.
• Electrical Sockets German Standard – 08 Pcs
• LAN Data ports RJ45 for PC – 1 Pc
• Telephone Outlets RJ11 – 1 Pc
• Oxygen Outlet: 2 Pcs
• Medical Air 4 Bar: 2 Pcs
• Vacuum Outlet: 2 Pcs
• I.V Pole – 1 Pc
• Basket for accessories.
10.a SINGLE ARM ANESTHESIA PENDANT Each
General Description - Ceiling mounted Anesthesia Pendant system, powder coated,

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Hygienically smooth surface, impact and disinfectant resistant. Extension arms made from
extruded aluminum section with specially formed five chamber system for extremely high
torsional strength. The pendant system has the flexibility to retrofit or exchange medical gas
outlets and electrical installations easily, without any need to demount the suspension arm
and service heads. Ceiling mounted supply unit consist of suspension arms, service head and
ceiling mounted components.
• Max. Degree of rotation at each arm:330- 350°
• Braking system: Electromagnetic/Pneumatic brakes to control horizontal movement.
• Electrical Sockets German Standard – 08 Pcs
• LAN Data ports RJ45 for PC – 1 Pc
• Telephone Outlets RJ11 – 1 Pc
• Oxygen Outlet: 2 Pcs
• Medical Air 4 Bar: 2 Pcs
• Vacuum Outlet: 1 Pcs
• Nitrous Oxide Outlet: 1 Pcs
AGS Passive
10.b DOUBLE ARM ANESTHESIA PENDANT
General Description - Ceiling mounted Anesthesia Pendant system, powder coated,
Hygienically smooth surface, impact and disinfectant resistant. Extension arms
made from extruded aluminum section with specially formed five chamber system
for extremely high torsional strength. The pendant system has the flexibility to
retrofit or exchange medical gas outlets and electrical installations easily, without
any need to demount the suspension arm and service heads. Ceiling mounted supply
unit consist of suspension arms, service head and ceiling mounted components.
• Max. Degree of rotation at each arm:330- 350°
• Braking system: Electromagnetic/Pneumatic brakes to control horizontal
movement.
• Electrical Sockets German Standard – 08 Pcs
• LAN Data ports RJ45 for PC – 1 Pc
• Telephone Outlets RJ11 – 1 Pc
• Oxygen Outlet: 2 Pcs
• Medical Air 4 Bar: 2 Pcs
• Vacuum Outlet: 1 Pcs
• Nitrous Oxide Outlet: 1 Pcs
AGS Passive
11 DOUBLE DOME LED OPERATING LIGHT WITH HD CAMERA WITH THIRD ARM
FOR MONITOR Each
Light System - High-performance LEDs of different chromaticity is provided for illumination
of the surgical site. The light head shall ensure shadow-free illumination while providing
deep-cavity light at the same time.
Mechanical Design - Ceiling-mounted operating light consisting of a ceiling tube, horizontal
tracking arm and spring arm with cardiac joint and a light head. The spring arm shall allow
full adjustability in height and unrestricted movability. Depending on site conditions (ceiling
structure) a ceiling anchor plate or an intermediate ceiling assembly shall be used for
mounting the light.
System Configuration - The system will consist of single ceiling suspension with 3 arms. Two
Arms for the light domes and third arm for the monitor to Hold 26’’ Monitor.
TECHNICAL SPECIFICATIONS:
 No. of dome: 2 (Main and Satellite)

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 Light Intensity Ec: 160,000 lx / 160,000 lx


 Light intensity adjustment: 10-100%
 Color temperature Tc (with adjustment): 3800 – 4800K
 Light field diameter d10 at Ec: 200-300mm
 Working range: 700-1400mm
 Illumination depth (L1+L2): 1200mm
 Color rendering index [Ra(1-8)]: >95
 Red color rendering index [R9] > 93
 Endo lighting with adjustable intensity: Green light
 Temperature of light surface after 60min: <40°C
 Increase of temperature near doctor’s head: <1°C
 Average service life of the LEDs (hours): >50,000
 Autoclavable Handles: Yes (3 Nos)
 Class of protection of light head: IP54

INTEGRATED HD CAMERA WITH HD MEDICAL GRADE MONITOR 27/34 Inch

12.1 ROUND/SQUARE or RECTANGULAR LAMINAR AIR FLOW CEILING SYSTEM Each


 2500MM or MORE FOR CIRCULAR LAF / 2500MM x 3000MM or MORE FOR
SQUARE/RECTANGULAR LAF Values are approximate.

The Laminar flow ceiling system has a round/square/rectangular base form to produce a
germ‐ and particle lean area through unidirectional homogeneous, low turbulence laminar
air flow. The system is specially designed and suited for the use in Operating room in
accordance with the international standards as mentioned in the specifications here below.
Air Distributor box: built of 2mm aluminum sheet, airtight welded. Varnish disinfectant
resistant bottom side completely varnished RAL 9010. Two rectangular ducts with flange for
fresh air supply, welded sidewise of the distribution box.
Filter grid: Tightly welded and additional on the connection grid‐side wall sealed with
polyurethane to pass the leak‐test. Both the air distributor box and the filter housing are on
the given sheet contact points totally gas‐tight welded (no sealing with silicon or something
similar).
Filter receptacle: All components for the receptacle of the filter element are made of
corrosion‐proof materials. Air tight welded filter intake made of aluminum, air tight
connected with the distribution box with 2‐component polyurethane. Compression
measuring connection for examining the pressure drop of the filter and the pressure drop
pipes are connected to the pressure drop manometers in the cabinet.
High efficiency particulate air filter: The filter medium consists of folded glass fibers‐filter
paper with thread range spacer, whereby the filter medium and the frame are closely
connected. The strong filter frame consists of aluminum and is equipped with an EPDM‐
profile washer. The filter exchange happens from the inside of the room after replacing the
CG‐Distributor frame.
Air distributor: CG distributor frame made of aluminum profiles; double sided covered with
special fabric; subdivided in separate large area elements; downwards removable.
Potential balance: The connection for the potential balance is mounted on the outside of the
air distributor box.
Bounding angle: The air distributor box has an integrated rotary connection angle for
connecting the intermediate ceiling.
TECHNICAL DATA

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 Total Air Flow:


6300 m3/h or better for Circular LAF
OR
8200 m3/h or better for square/rectangular LAF
 Air Velocity: 0.25 m/s
 Filter Class to EN 1822: H14 | 99.998%
 Filter Dimensions: 2 pcs. 1100 x 762 mm and 4pcs. 915 x 610 mm
 Total active filter area: 94 m2
 Initial Pressure drop: 115 Pa
 Final Pressure drop (Recommended): 240 Pa
 Height: 350mm-450mm
12.2 ANGULAR EXTRACTION WALL ELEMENT WITH AIR GRIDS (2 PER OT) Each
 The air grills is made of Stainless Steel, 135° Partition element.
 The fluff separator is made of stainless-steel wire mesh in accordance.
 Include air grids of standard 400x400 or as per design included the cut outs and wall
panels reinforcements
 Correct air extraction grids as per appointed MEP engineer’s recommendation, including
galvanized steel air duct dim. 470 x 300mm fully accessible with upper circular connection
diam.150mm
13 DEDICATED HYGENIC AIR HANDLING UNITS (Euro vent/ Cetiat / Equivalent Each
certified). Each
● Local provision for the theaters (if already not installed HVAC System)

● Fan Type: Plug-fan


● Filter: At least three stage filtration in AHU G4, F9 and F7
● Fan effeciency: 70% or batter
● Temperature range adjustable for heating and cooling.
OR as per drawing or actual requirement of the hospital
● Unit should have humidification & Dehumidification Provision built in or
equivalent.
● Constant air flow control.
● Unit should be design criteria 70% regulated air and 30% of fresh air.

● Casing should be water proof.


● Ambient temperature as site (I/O to specify at the finalizatio of biding documents).

● RH Factor built in or equivalent.


● Temperature regulation 20 to 26 degree.
● Technical Date Sheet/Scheduled will be provide along with the bid.

Surgeon Stool Panel


● Touch Screen Provides visual information about the current status of the
monitored operating theatre systems and allows controllong and setting of the essential
physical. Latest Type 20-25" TFT/LCD Display.
Control & Monitoring
● Room Ceiling lighting Control (On/Off Dimming, White & RGB)

● Digital Clock and Stopwatch.

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14. 14 AUTOMATIC WATER DISPENSER FOR SCRUB AREA


Clinical Purpose: Clean area for scrubbing of surgeons and nurses.

TECHNICAL DATA
Three stations knee operated scrub staton Madeof stainless steel.
Anti Splash basin.
1/2-siphon
Removable or fixed front panel
IR Sensor and 3-knee controls.
3-water tapes with a mixing valve. Water pipe
hoses for cold and hot water.
stainless steel brackets or fittings to fix the sink to the wall.
Hygenic tap shaving built-in-tap thermostatic mixing valve to supply 42◦C hot water.

The tap shall also have built-in strainers and the provision for easy and quick thermal
disinfection to remove the scaling.
"Accessories:
● Soap dispenser unit.
● Hand washing brush dispenser made of SS"
15 4K VIDEO MANAGEMENT & DOCUMENTATION SYSTEM: AUDIO VIDEO
MANAGEMENT, DOCUMENTATION & COMMUNICATION (2 WAY AUDIO AND 1
WAY VIDEO) to be quoted as Optional Optional
Each
General Description: AV System is a modern, lightweight and interconnecting OR
integration solution, comprising of the modules Advance data archiving. The system offers
4K UHD A/V distribution inside the OR, documentation and audiovisual communication
within the hospital environment, designed to be operated from the most compact device in
its class. Due to its minimal footprint, system enables new possibilities of profiting from the
benefits of OR integration without the infrastructural investment
of traditional, hardware-intense products. It comprises of 3 main components.
 A/V Management Video distribution in the operating room – in 4K UHD, 3D and FULL
HD.
 Documentation Content management in up to 4K UHD – from the endoscope to the
HIS.
The system image chain provides brilliant surgical image quality and content management in
up to 4K UHD, from the endoscope to the Hospital Information System. integrated system
ensures connectivity and management of all its elements - cameras, video sources, monitors
and network connected Participants.
Experience real time communication with collaboration partners within the hospital
network. Benefit from high definition video streaming to share the surgical image with other
consultants or an auditorium in a secure and privacy protected environment. Seamless
communication is ensured with onboard audio talkback function. Emphasize important
anatomical or pathological structures with live video annotations.

Telestration on the touchscreen inside the OR can be used to visually annotate the streamed
image. Get important consultation of another expert during the surgery

Knowledge sharing Medical education takes time. Share procedures intraoperatively


beyond the OR.

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The most important features at a glance:


 Best-in-class image chain in brilliant 4K UHD, 3D and FULL HD from endoscope to
monitor, providing near to zero latency.
 Powerful audiovisual communication function. Video streaming and audio talkback
with bidirectional telestration.
 Compact and service friendly design.
 Flexible 8x8 video management system in 4K UHD, 3D and FULL HD including
PiP/PaP functionality.
 Fully integrated documentation solution in up to 4K UHD.
 Data security through automated data transfer via HL7 and DICOM.
 User-friendly and Intuitive Graphic User Interface within integrated Smart Screen
or separate touch screen.

Technical data
Video inputs: 5x 12G SDI / 3x HDMI 2.0
Outputs: 6x 12G SDI / 2x HDMI 2.0
USB: 4x USB 3.0 / 1x USB 2.0
LAN: 2x Ethernet
Audio: 1x Audio in / 1x Audio out
Remote control: 2x ACC
Input voltage: 100-240 VAC
Input frequency: 50-60 Hz
Input frequency: 50-60 Hz
Max. input current: 2.5 A (@100 VAC), 1 A (@240 VAC)
Operating mode: Continuous Operation
Degree of protection: IPx0
Protection class: I
Dimensions: 305 x 74.5 x 355 (W x H x D)
Weight: 4 kg

Technical data for Data Image Archiving System


Video inputs: 1x DP 1.2a / 1x HDMI 2.0
Outputs: 1x DP 1.2a / 1x HDMI 2.0
Interfaces: DICOM, HL7
Input voltage: 100-240 VAC
Input frequency: 50-60 Hz
Output power: 250-300 Watt
Image formats: BMP, JPG, JPNG
Video formats: MPEG-4, MPEG-2, MOV
Dimensions: 305 x 74.5 x 355 (W x H x D)
Weight: 6 kg

16 HEPA CEILING DIFFUSERS WITH HEPA FILTERS FOR CLEAN CORRIDOR Each
Designed to provide air filtration and distribution in one unit Viruses, bacteria and dust
particles are filtered out of the airstream immediately before the air outlet, eliminating the
risks associated with central system filtration, such as cross contamination in the ventilation
ducts. Filtrasept is ideal for use wherever clean air or a germ‐free atmosphere is needed,
such as Operating Theatres, Treatment Rooms, Intensive Care Units, Sterile Zones and

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Isolation Areas.
TECHNICAL DATA
 Housing RAL 9010 powder coated
 Connection for pressure drop measurement / DEHS test
 Connection for filter tight test
 Ceiling supporting angle
 Perforated Plate Diffuser
 HEPA filter type CR‐VS‐H14 557 x 557 x 75

LOCAL WORKS TO BE EXECUTED WITH PROCUREMENT OF MODULAR OPERATION THEATERS


17 HVAC DUCTING WORKS COMPLETE IN ALL ASPECTS SqFt.
HVAC DUCTING WORKS ( job 1)
All duct work shall be of galvanized steel sheet unless otherwise indicated on
Drawings. Galvanized steel shall be of lock forming quality (LFQ) and shall have a
galvanizing coating of 245 grams (G80) total for both sides of one square meter of
sheet with regular spangles. The G.I. sheet shall conform to ASTM A-924 and
ASTM-90.
Structural Steel shall be M.S. members rolled from Pakistan Steel billets or
equivalent.
Fabrication, Installation, Insulation, testing and commissioning of GI sheet metal
duct work complete in all respect with hangers, supports, bracing and fixing
accessory in accordance with the final approved ducting drawing.
Ducting: GI Sheet: 22 AWG
Cladding: GI Sheet: 24 AWG
Volume Control Damper: GI 18 AWG
Grills & Diffusers: GI 18 AWG
INSULATION
Polyolefin Rolls and Sheets should be made of closed cell cross linked polyolefin foam that
controls
condensation, has high thermal efficiency and sound absorption. They should be made up of a
sandwich product that is composed of foam, alupet foil and self-adhesive backing

TecHnical Specification (For Inner Duct)


Fire rated “CLASS 0” as per BS 476 Parts 6 & 7
Thickness 12mm
Very low water vapor permeance (0 perms)
Water tight due to the pre-applied Alupet foil
High thermal efficiency (λ[W/(m•k)] 0.032 – 0.035
(23 °C – 45 °C)
Wide temperature range (from -50 ˚C to +105 ˚C)
Chemical resistance – resistant to most chemicals (sodium, silica, fluoride, chloride, etc.
Antibacterial & antifungal
Environmental friendly – ODP = 0 and GWP < 5
Very low VOC emission level ( < 4 μg/m2/hr in 24 hours)
Good mechanical resistance
Sound absorption properties
Easy and fast to install
Aesthetical look

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OUTER DUCT INSULATION:


Insulation foam should be made of closed cell cross linked polyolefin coated with a strong and
durable
jacketing which replaces costly and complex aluminum, zinc plated steel or stainless-steel
sheet facings
UV and corrosion resistance
Fire rated “CLASS O” as per BS 476 Parts 6 & 7
Thickness : 25mm
Very low water vapor permeance (0 perms)
Water and water vapor resistant
Very low water absorption rate (<0.11% by volume)
High thermal efficiency (λ[W/(m•k)] 0.034 – 0.036
(24 °C – 46 °C)
Wide temperature range (from -80 ˚C to +100 ˚C)
Chemical resistance – resistant to most chemicals (sodium, silica, fluoride, chloride, etc.)
Antibacterial & antifungal
Environmental friendly – ODP = 0 and GWP < 5
Very low VOC emission level ( < 4 μg/m2/hr in 24 hours)
Good mechanical resistance
Easy and fast to install
Aesthetical look
VOLUME CONTROL DAMPER
A substantially constructed manual volume control damper of the butterfly or multiple blade
type as per latest SMACNA Duct Construction Standards shall be fitted where shown on the
Drawings and at all branch entries or exits with main ducts for balancing purposes. Dampers
shall have galvanized interlocking blades of 8 inches (200 mm) maximum blade width. Blades
shall be fabricated from 16 gauge steel with seamed edges and a maximum length of 4 feet.
Volume control Dampers shall have parallel or opposed blades. It should be noted that these
dampers shall be separate and independent from the dampers, hereinafter specified. Volume
Dampers are not required where splitters Dampers, as specified hereinafter, are installed.
Fire Dampers
Fire dampers are to be installed as shown on the Drawings. Frames shall be 100 mm x 25 mm
x 3 mm (4” x 1” x 1/8”) galvanized steel channel with 16 gauge thick blades. Blades shall have
an overlay of 1” and shall be fixed on bronze type bearings. Dampers shall be complete with
linkage rod and fusible link rated at 160o F (71o C). Damper construction shall meet NFPA
90-A, requirements.
AIR INLET & OUTLET DEVICES
All grilles, registers, diffusers and louvers shall be of extruded aluminum anodized and
powder coated in approved color
LOCALLY SUPPLIED OF BEST QUALITY
18 AUTOMATIC CONTROL SYSTEM (to be quoted as Optional) JOB
This Section includes Control System for HVAC works and components, including open
protocol control components for terminal units:
All work described in this section shall be installed, wired, circuit tested and calibrated by
factory certified technicians qualified for this work and in the regular employment of
authorized local agent with minimum of 5 years of installation experience with the
manufacturer. Supervision, calibration and checkout of the system shall be by the trained
engineers of the local agent. The work under this section consists of supply, installation,
testing and commissioning of complete Microprocessor based Control System stated herein
and/or as required for the project.

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All labour, material, equipment and software necessary to meet the functional requirement of
the system as specified herein shall be included in the scope of work. Drawings are
diagrammatic only and all controls, materials, etc. not shown but necessarily required to
meet the functional intent shall be provided without any additional cost to the Owner. All
wiring in connection with the automatic control system shall be as per manufacturer's
recommendations. The term "wiring" shall be construed to include furnishing of wiring
conduiting, miscellaneous material and labour as required for mounting and connection of
the electrical control devices. The control manufacturer shall furnished.
LOCALLY SUPPLIED OF BEST QUALITY

19 FOUNDATION PAD FOR HVAC EQUIPMNT (Civil Works) will be provided SqFt
free of cost by the firm

All foundation related civil work shall include in this scope of work. Providing, laying of crock
sheet 25mm thick, reinforcement for foundation structure and foundation construction work
as per drawing
LOCALLY SUPPLIED OF BEST QUALITY

20 ELECTRICAL WORKS SqFt


ELECTRICAL WORKS FOR HVAC
Electrical Contractor shall provide power supply (Normal or Normal + Emergency) at MCCs,
ACPs and DBs in HVAC Plant Room AHU Rooms. From these points onwards all electrical
works related to equipment controlled from MCC, ACPs and DBs shall be done by HVAC
Contractor. Connection of incoming cables terminated at MCCs, ACPs and DBs with respective
panels shall be in scope of Electrical contractor. Sizes of cables shall be as per approved
equipment technical schedule or data sheet.

ELECTRICAL WORKS FOR OPERATION THEATHERS

Electrical Contractor shall provide all cabel works for the equipment to be installed in
operation room in respect to the load requirement of the OR.

LOCALLY SUPPLIED OF BEST QUALITY

21 INSTRUMENT AND GUAGES Each

PRESSURE GUAGE
Pressure gauges shall be of the phosphor bronze Bourdon tube type. Dial diameter shall be
4½” (114 mm) and shall permit easy reading from flow with black numerals on non-
reflecting white metal dial face. Pressure gauges shall be complete with shut-off cock and
Snubber. Tubes and necessary tubing with socket adapter. The accuracy of pressure gauges
shall be + 1%.
Thermometers
Thermometers for water line shall be industrial mercury type with die-cast aluminum case, 9
inch (225 mm) adjustable stem. Thermometers shall be complete with well for piping. The
thermometers shall have dual calibrations in o F and o C. Thermometer for ducts shall be
remote bulb dial type with stainless steel bulb. Separable stainless steel socket 3/4” (19 mm)
connection with bronze armored capillary shall be provided. Dial size shall be 5” (127 mm)
and 3” (76 mm) for ceiling mounted AHUs. Thermometers shall have dual calibrations in

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degrees Fahrenheit and centigrade with suitable increments. Range shall place operating
temperature at or near the middle of scale. Range shall not be less than one and half times the
maximum temperature. The accuracy of thermometers shall be + 1%. Thermal grease shall be
filled in thermometer wells to ensure to correct sensing of temperatures.
LOCALLY SUPPLIED OF BEST QUALITY

22 ALUMINUM WASHABLE FILTER FOR FRESH AIR Each


Filter media shall be aluminum screen, arranged in alternate layers of flat and herring bone-
crimp, 4 layers of each per inch, rod reinforced and enclosed in a frame of 16 gauge
galvanized steel with flush mitered corners.
Pressure drop at 500 fpm (2.5 m/s) velocity shall not exceed 35 Pa. Holding frames shall be
factory built of 16 gauge steel with felt air seal. Filters shall have atleast 35% efficiency on 0-5
micron range when tested in accordance with ASHRAE Standard 52.

Panel filters for AHUs shall be 2-inch-thick. Panel filters for all ventilation fans (supply air
fans) and outside Air Intake Louvers shall also be 2 inch thick.

LOCALLY SUPPLIED OF BEST QUALITY

NOTE:
 The system should be FDA/CE/JIS/MHLW/Eurovent/AHRI/ISO7/ISO5 approved was added in the
specifications.
 Country of Origin was added as USA, Europe and Japan.
 05 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation and validation of the equipment.

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S. No. 3 (OT Equipment)


3.1 STERNUM SAW BATTERY OPERATED
Clinical
Cardiac Surgery
Specialty
Generic
Sternum Saw/Bone Mill/Drill
Name
Clinical A sternal saw is a bone cutter used to perform median sternotomy, opening the
Purpose patient's chest by splitting the breastbone, or sternum.
TECHNICAL SPECIFICATIONS
The sternum saw can also be used as a reciprocating saw and can be equipped with
various lengths of sternum attachments.
Sternum saw with protection sleeve and keyless chuck with continuously adjustable
rotation speed and switch lever from Step 1 to 2. Basic model can be used as
reciprocating saw. Rotate the attachment/chuck to the desired position. Locking always
at 90°.
Precise cutting guide with good visibility condition
Easy clamping of saw blade (no tools required)
Attachment of protection sleeve in 4° different positions possible (locking at 90°)
Power pack, newest Li-Ion technology.
Includes control unit, battery, electronics and motor – all united in one Power pack
Automatic recognition of the performance parameters according to the used hand piece
no need to sterilize delicate components
Latest battery technology – long lifetime no memory effect
Display for battery charging status: green, orange, red (discharged) with Withe LEDs for
additional illumination of the OR field
One bay charger with power cord
Rinse adapter for sternum saw
Key less top sternum saw
Sternum saw blade (50 pcs)
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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3.2 DELIVERY TABLE

Clinical
Gynecology
Specialty
Generic
Delivery Table/Deliver Bed
Name
Clinical
Purpose Delivery table is widely used for obstetric birthing, gynecology examination and operation.

TECHNICAL SPECIFICATIONS
Backrest adjustment by gas spring
Trendelenburg and reverse Trendelenburg to be quoted as Optional by gas spring
Height adjustment by foot pedal
Anti-microbial, water proof, flame retardant, air permeable mattress
Removable footrest mattress
Stainless steel handles
Stainless steel waste bin
Lockable, adjustable and removable side rails
Removable and Adjustable Polyurethane Thigh Supports
Lockable castors
Protective plastic bumpers
Detachable head board
Height adjustable IV Pole
ABS/HPL covered sub-frame
Stainless steel accessory rails
Easily cleanable, compact laminate mattress platform
Electrostatic powder coated metal frame
IV pole sockets
TECHNICAL DETAILS
External Dimensions: min: 80x155cm max: 80x187cm
Bed Surface: 60x168cm
Height (without mattress): 62-91cm
Backrest Angle: 0o-70o
Trendelenburg Angle: 0o-15o
Reverse Trendelenburg Angle: 0o-15o
Castor Diameter: 125mm
Safe Working Load Capacity: 240kg
Mattress Thickness (backrest and pelvic sections) 8cm
Footrest Mattress Thickness: 12cm
Under bed Clearance: 17cm
NOTE:
 The system should be FDA/CE/JIS/MHLW approved and 01 certificate is required
mandatory.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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3.3 ORTHOPEDIC TRACTION TABLE

Clinical Specialty Operation Theater


Generic Name Traction Table for Orthopedic
Clinical Purpose Orthopedic tables include specific apparatus for supporting and/or providing traction for
the patient's limbs during orthopedic procedures. Applications for these tables include both upper-extremity
procedures.

TECHNICAL SPECIFICATIONS
The table top should be 100% radiolucent material & X-Ray access
5 Section table plate or better
Load capacity should be no less than 400kg or better
The table pad should be double layered and not soft but can be molded by the figure of the patient to deliver
even counterforce and reduce the possibility of ulcer, and it should be water-proof and anti-static material and
can be washed by water directly; each joint should be sealed by ultrasonic not glue and sewing.
The thick of mattress should be more than 66.5mm
Remote Control Operated
It should have a battery inside the table, which can work 50-80 operations for two weeks and the battery should
be standard configuration.
It should have electric longitudinal shift function not less than 300mm or better.
It should have an build-in elevator.
The rails & the column of the table should be made of high level of aluminum alloy.
Length of the table >2050 mm or better
Width of the table with rails >500 mm or better
The thickness of mattress >75mm or better

Electric Function
The lowest position >750 mm or better
The highest position <1000mm or better
Longitudinal shift > 300 mm or better
Turn left > 20° or better
Turn right > 20° or better
Trendelendburg position > 30° or better
Reverse Trendelendburg position > 30° or better
Back plate up position >75° or better
Back plate down position > 38° or better
Flex position >210° or better
Re-flex position > 100° or better

Mechanical Function
Head plate up > 45° or better
Head plate down > 90° or better
Build-in elevator > 120 mm or better
Leg plate up >20° or better
Leg plate down >90° or better
Leg plates spread > 180° or better

Accessories
A pair of arm boards with 2 clamps & 4 bands, and it has the universal coupling for up & down & rotary function.
Anesthesia frame with 2 tubes & 1 clamp.

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Orthopedics Extension accessories


Trolley for the whole Orthopedics extension accessories
One piece of pelvis plate with radiolucent material
Adaptor for connecting the pelvis plate with the operating table
One counter traction post
One leg support (Pair)
One traction boot (Pair)
One traction screw device with support bar
A pair of Elongation bar with articulation combined the long side with short side.
Other accessories for prone position of orthopedics

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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3.4 HD ARTHROSCOPY SYSTEM

Clinical Specialty Operation Theater


Generic Name Arthroscopy System
Clinical Purpose It should provide an outstanding and stable visual field down to details,
creating an excellent visualizing experience for the surgeons with true-to-
color images, enabling easier and finer operations.
TECHNICAL SPECIFICATIONS
Should be equipped with a CMOS image sensor, the image color, edge and structure are
optimized, the noise minimized. It should provide an outstanding and stable visual field
down to details, creating an excellent visualizing experience for the surgeons with true-
to-color images, enabling easier and finer operations.
4K system that should support 3840 x 2160 resolution or better, that should provide
much more information than conventional HD.
No details are lost even if it is zoomed at 2.0X.
3-CMOS image sensor, supporting 60FPS 4K resolution digital signal
Camera Head
Lens mount: C-mount
CMOS image sensor x3
Magnification ratio: Focal lens 16-32 mm
Chromoendoscopy technology
White Balance adjustment
Snap/Record function
Customizable HEAD B switch function
Customizable +/- buttons function to choose from Brightness adjustment, Edge
enhancement, Image magnification or Contrast enhancement
Image Processor
Resolution 3840*2160p@60fps or better
Storage USB, snap to export
Video output signal: DVI*2, HD-SDI*2, Y/C*1, CVBS*1
Digital zooming: 2-times , 3-step setting or better
White balance: Auto and memory
Image enhancement: Edge enhancement
IRIS: Auto/Peak/Average
Light Source
Lamp: 2-LED
Brightness: Level 1-19
Light modes: WL / VIST / NBI or equivalent.
Standby mode: Low illumination
Lamp life: ≥10,000 hours or better
Mechanical features: Low heat, low noise
Illumination Cable
Total length(mm,±5%): 3000 or better
Dimensions of light input surface (mm,±10%): Diameter:5.4 Lengt:62 or better
Dimensions of light output surface (mm,±10%): Diameter:5.3 Lengt:16.0 or better
Light output angle (°,±10%): 40 or better
Spectral transmittance(420-720nm) ≤35% or better
Light transmittance(420-720nm) ≤20% or better

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Medical Grade Monitor:


30’’ Inch or better LED backlight monitor
Resolution 3840(RGB)x 2160 or better
Colour support 1.0 Billion or better
Contrast ratio (min) 900:1 or better
Viewing angle L/R 178° Typ, U/D 178° or better
Signal input DVI/SDI/HDMI/DP
Signal output DVI/SDI

Trolly from Manufacture:


Trolley made of Metal and molded fiber
Four antistatic wheels with individual brakes
White balance cap mounted on trolley
Isolation transformer should be available
Adjustable scope hanger
Light guide connector holder
Adjustable shelf height
Swivel monitor hanger
 Sheath price to be quoted as optional.
 Shaver System to be quoted as mandatory,
 Fluid System to be quoted as mandatory,
 RF/HF Generator to be quoted as mandatory.

Rigid Endoscopes Arthroscopes:

1: Outer dia: 4mm, working length: 175mm, Direction of view: 0° or better


2: Outer dia: 4mm, working length: 175mm, Direction of view: 30° or better
3: Outer dia: 4mm, working length: 175mm, Direction of view: 70° or better
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.5 ELECTRO HYDRAULIC OPERATION TABLE


Clinical Specialty Operation Theater
Generic Name Operation Table
Clinical Purpose This table is used for the patients who are going under surgery which is
electro-hydraulically controlled by buttons and remote control to make
different position easy for surgical procedures.
S.NO. TECHNICAL SPECIFICATIONS
It shall be battery powered and electric /electro-hydraulic operating table.
It shall have load of at least 450 kg guaranteeing highest safety and stability.
The table top should be radiolucent material & X-Ray access.
It shall be with modular design tabletop that enables it to be tailored for various
surgical discipline needs.
It shall be with a hook and One-Click Connection Design to just one click to change
table components module.
It shall be with a modular recognition system and intelligent anti-collision system
to avoid table components collision during movement. It shall recognize the type of
the table component and match the anti-collision data automatically.
The table pad should be double layered and not soft but can be molded by the
figure of the patient to deliver even counterforce and reduce the possibility of
ulcer, and it should be water-proof and anti-static material and can be washed by
water directly; each joint should be sealed by ultrasonic not glue and sewing.
The thick of the mattress should be more than 75mm or better
It shall be with dual-joint leg plate and dual-joint head plate.
It shall be having 3 control models including remote panel, column panel and foot
switch.
The rails and table main frame shall be made of Stainless Steel. And the column
cover shall be made of Stainless Steel 304.
It shall have the "fiber-class reinforced plastic" material as the cover of the table
base not metal to avoid the potential shocking by the current.
It shall have a battery inside the table, which can work 50 operations or better and
the battery should be standard configuration.
It should be interchangeable for the leg plates and head rest for normal position
and reverse position
It should have electric longitudinal shift function not less than 450mm or better for
free access to C-arm.
It shall be with the table positions memory that can save more than 10 positions or
more, so the user can select the memorized positions for the specific surgery freely
without complex adjustment.
It shall have the electric-hydraulic movements including table up and down, back
up and down, turn left and right, Trendelenburg and reverse Trendelenburg, leg
plate up & down, which shall be controlled by hand control panel.
It shall support automatic reset to zero position by pressing one button (leveling
function). It also shall be with Flex, reflex position by pressing one button.
4 Castors shall be electrically locked firmly / unlocked by using the hand control.
The remote hand control shows the information on the display, such as
movements, battery, brake, anti-collision information, etc.
The remote hand control shall be with the backlight for operating in a dark
environment

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The hand control shall control the electric movement of leg plate individually and
simultaneously.
Technical Specification
Length of the table (main unit) = 950 mm or better
Width of the table with rails =590 mm or better
Electric Function
The lowest position ≤ 580 mm or better
The highest position ≥ 1070 mm or better
Longitudinal shift ≥300 mm or better
Turn left ≥ 26° or better
Turn right ≥ 26° or better
Trendelenburg position ≥ 35° or better
Reverse Trendelenburg position ≥ 35° or better
Back plate up position ≥ 90° or better
Back plate down position ≥ 45° or better
Flex position ≥220° or better
Re-flex position ≥ 110° or better
Leg plate up ≥ 80° or better
Leg plate down ≥ 100° or better
"0"position by one electric button
Mechanical Function
Head plate up ≥ 60° or better
Head plate down ≥ 60° or better
Leg plates spread ≥ 180° or better
Accessories
Anesthesia frame
Head support with divided version pad & adaptor connecting with the table
A pair of leg supports with 2 clamps, pads & bands, and it has the universal
coupling for up & down & rotary function
A pair of arm boards with 2 clamps & 4 bands, and it has the universal coupling for
up & down & rotary function
NOTE:
 The system should be FDA/CE/JIS/MHLW approved and 01 certificate is
required mandatory
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the
supplier in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment.

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3.6: A. C-ARM (IMAGE INTENSIFIER)


Clinical Specialty Operation Theater
Generic Name C-Arm
Clinical Purpose A Versatile, compact and true counterbalanced C-arm unit should allow un-
obstructed Positioning and enhanced ease of operation in OT for surgical interventions.
S.NO. TECHNICAL SPECIFICATIONS

Mechanical motion requirements for C-Arm:


Motorized Vertical travel: Minimum 40cm or more
Horizontal travel: 18cm or better
Rotation of C-arm: +/- 120 deg. or more with safety stop.
Source to Image intensifier distance (SID): 95 cm or more

Image Intensifier
should have at least triple field 9” input diameter or better
having entrance screen of Cesium Iodine
TV camera should be of high resolution at least 1k x 1k or more.
TV camera type should be CCD
Image rotation should be digital having reversible option as well.

X- ray generator:
At least 15 KW or even better
Max X-Ray tube current 120 mA or better
Max X-ray tube Voltage 110kv or better

X-Ray Tube
X-ray tube of dual focal spot 0.5 and 1.5 (300 KHU) or better.
Must have rotating anode
X-ray tube voltage 110kv or better
Should have inherent filtration
Collimators should have side shutters

Fluoroscopy output:
40-110 KV or better
Low dose management system
mA range 0.1 to 9 mA or better on low dose
mA range 0.2 to 18mA or better on continuous

Image processing:
Two 19˝ or better LCD monitors for diagnostic image quality display with one 7inches or more touch
screen for better handling.
Resolution should be 1280 x 1024 pixels or better
The system should have automatic dose level selection.
Contrast ratio should be 500:1 or more
Maximum light output 500 cd/m2 or more
Image storage of 10000 images or more.
It should have image annotation facility; measuring of distances and angles, support of DICOM 3.0
functions.
System must have DSA with 30fps

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NOTE:
• The system should be FDA/CE/JIS/MHLW approved.
• 03 years with parts and services comprehensive warranty.
• Life span of the quoted model should be clearly defined by the manufacturer.
• Technical training as well as operational training must be provided by the supplier in case if
required.
• Service manual as well as operational manual must be provided along with the machine.
• PPM Schedule should be share with Biomedical Engineering Department along with the supply
of equipment, which will include calibration and vailidation of the equipment.

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3.6:B: C-ARM (IMAGE INTENSIFIER)WITH FLAT PANEL DETECTOR

Clinical Specialty Operation Theater


Generic Name C-Arm
Clinical Purpose A Versatile, compact and true counterbalanced C-arm unit should allow un-
obstructed Positioning and enhanced ease of operation in OT for surgical
interventions.
S.NO. TECHNICAL SPECIFICATIONS

Mechanical motion requirements for C-Arm:


Motorized Vertical travel: Minimum 40cm or more
Horizontal travel: 18cm or better
Rotation of C-arm: +/- 120 deg. or more with safety stop.
Source to Image intensifier distance (SID): 95 cm or more

Image Intensifier
should have at least triple field 9” input diameter or better
having entrance screen of Cesium Iodine
TV camera should be of high resolution at least 1k x 1k or more.
TV camera type should be CCD
Image rotation should be digital having reversible option as well.

X- ray generator:
At least 15 KW or even better
Max X-Ray tube current 120 mA or better
Max X-ray tube Voltage 110kv or better

X-Ray Tube
X-ray tube of dual focal spot 0.5 and 1.5 (300 KHU) or better.
Must have rotating anode
X-ray tube voltage 110kv or better
Should have inherent filtration
Collimators should have side shutters

Fluoroscopy output:
40-110 KV or better
Low dose management system
mA range 0.1 to 9 mA or better on low dose
mA range 0.2 to 18mA or better on continuous

Image processing:
Two 19˝ or better LCD monitors for diagnostic image quality display with one 7inches
or more touch screen for better handling.
Resolution should be 1280 x 1024 pixels or better
The system should have automatic dose level selection.
Contrast ratio should be 500:1 or more
Maximum light output 500 cd/m2 or more
Image storage of 10000 images or more.
It should have image annotation facility; measuring of distances and angles, support of

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DICOM 3.0 functions.


System must have DSA with 30fps

FLAT PANEL DIGITAL X-RAY DETECTOR (FPD) (2NOS)


17x17” Cesium Iodide (Csl) with Amorphous Silicon or better
Pixel Matrix: 3000 (H) × 3000 (V) or better
Pixel Pitch: 150μm or less
DQE: > 70 % or better
A/D Conversion: 14 bit or better

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.7 FULL HD LAPAROSCOPY SYSTEM


Clinical Specialty Operation Theater
Generic Name Laparoscopic System
Clinical Purpose Laparoscopic system is used for surgical procedure without opening the body
in an efficient and specialized way.
S.NO. TECHNICAL SPECIFICATIONS
Should be equipped with a CMOS image sensor, the image color, edge and structure are
optimized, the noise minimized. It should provide an outstanding and stable visual field
down to details, creating an excellent visualizing experience for the surgeons with true-
to-color images, enabling easier and finer operations.
4K system that should support 3840 x 2160 resolution or better, that should provide
much more information than conventional HD.
No details are lost even if it is zoomed at 2.0X.
3-CMOS image sensor, supporting 60FPS Full-High-Definition (FHD) digital signal

Camera Head
Lens mount: C-mount
CMOS image sensor x3
Magnification ratio: Focal lens 16-32 mm
Chromo endoscopy technology
White Balance adjustment
Snap/Record function
Customizable HEAD B switch function
Customizable +/- buttons function to choose from Brightness adjustment, Edge
enhancement, Image magnification or Contrast enhancement

Image Processor
Resolution 3840*2160p@60fps or better
Storage USB, snap to export
Video output signal: DVI*2, HD-SDI*2, Y/C*1, CVBS*1
Digital zooming: 2-times , 3-step setting or better
White balance: Auto and memory
Image enhancement: Edge enhancement
IRIS: Auto/Peak/Average

Light Source
Lamp: LED
Brightness: Level 1-19
Light modes: WL / VIST
Standby mode: Low illumination
Lamp life: ≥10,000 hours or better
Mechanical features: Low heat, low noise
Illumination Cable
Total length(mm,±5%): 3000 or better
Dimensions of light input surface (mm,±10%): Diameter:5.4 Lengt:62 or better
Dimensions of light output surface (mm,±10%): Diameter:5.3 Lengt:16.0 or better
Light output angle (°,±10%): 40 or better

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Spectral transmittance(420-720nm) ≤35% or better


Light transmittance(420-720nm) ≤20% or better

Medical Grade Monitor:


30’’ Inch or better LED backlight monitor
Resolution 3840(RGB)x 2160 or better
Colour support 1.0 Billion or better
Contrast ratio (min) 900:1 or better
Viewing angle L/R 178° Typ, U/D 178° or better
Signal input DVI/SDI/HDMI/DP
Signal output DVI/SDI

Trolly from Manufacture:


Trolley made of Metal and molded fiber
Four antistatic wheels with individual brakes
White balance cap mounted on trolley
Isolation transformer should be available
Adjustable scope hanger
Light guide connector holder
Adjustable shelf height
Swivel monitor hanger

Rigid Endoscopes:

1: Outer dia: 10mm, working length: 344mm, Direction of view: 0° or better


2: Outer dia: 10mm, working length: 344mm, Direction of view: 30° or better
3: Outer dia: 5mm, working length: 312mm, Direction of view: 0° or better
4: Outer dia: 5mm, working length: 312mm, Direction of view: 30° or better
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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3.8 FULL HD VIDEO ENDOSCOPY SYSTEM


Clinical Specialty Operation Theater
Generic Name Endoscopy System
Clinical Purpose It provides a clear and bright image contrast that allows a better vision of
mucosa and blood vessels in the GI tract.
S.NO. TECHNICAL SPECIFICATIONS

Full HD (1920*1080p) Video Endoscopy system:


Full High Definition Video Processor & Light source
Brilliant, Full high-definition (1920*1080) HD images for a clear and more detailed
visualization.
It should be HD Digital/optical Video and Image Processor.
Chromo-endoscopy technology combined with optical/digital image processing. It
provides a clear and bright image contrast that allows a better vision of mucosa and
blood vessels in the GI tract.
Zoom: ×1, ×1.4,×1.6,×1.8 or better
White Balance Adjuster, USB Ports, image enhancement, freeze scan & integrated or
separated video recorder with 500GB storage capability or better.
Patient data management software from same manufacturer or better.
Outputs: HD-SDI, DVI, VGA, S-Video & CVBS
Light source (Integrated/Separated):
Main Lamp Xenon life span: 500 Hrs or better
Auxiliary lamp LED/Halogen should be available

HD Medical Grade Monitor


HD Medical Grade Monitor
26" inch Medical Grade or better.
Aspect ratio of 16:9 or better
With all standard accessories

High Definition Gastrointestinal Scope


High definition gastrointestinal video scope with advanced technological features.
Water Jet function.
Field of View 140 degree or better
Direction of View: Forward Viewing
Depth of field 3-100 mm or better
Insertion tube outer diameter 9.8 mm or better
Channel inner diameter 3.2 mm or better
Bending Section up 210°, Down 90° or better
Right 1000 Left 1000 or better
With Standard Set of Accessories.

High Definition Colono Video Scope:


High definition Colono video scope with advanced technological features.
Water jet function.
Forward Viewing, Field of View 1400 or better
Depth of field up to 3-100 mm or better

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Insertion tube outer diameter max 12.5 mm or better


Channel inner diameter 3.8 mm or better
GDF/HFT/RIT/PB to facilitate colonoscopy and increase patient compliance.
Angulations Up 180°, Down 180°, Right 1600 , Left 1600 or better
Forward Water Jet Function.
With all standard accessories.

Endoscopic Cart/Trolley (From the Manufacturer)


Compatible with above Endoscopes/system
Erosion free durable material
Should have castors with brakes

Endoscopic storage cabinet (Supplied Locally)


Compatible with above Endoscopes
Front opening/with complete fittings
Should have capability to store 5 endoscopes

Endoscopic disinfector (Supplied Locally)


Automatic disinfection system & should be able to clean all external/internal surfaces
of endoscopes.
Compatible with quoted endoscopes.

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment.

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3.9 MOBILE OPERATION THEATER LIGHT


Clinical Specialty Operation Theater
Generic Name Mobile OT Light
Clinical Purpose LED Surgical lights illuminate the surgical site for optimal visualization of
small, low-contrast objects at varying depths in incisions and body cavities
S.NO. TECHNICAL SPECIFICATIONS
DESCRIPTION OF FUNCTION
LED Surgical lights illuminate the surgical site for optimal visualization of small, low-
contrast objects at varying depths in incisions and body cavities.
GENERAL REQUIREMENTS
The light shall adopt latest LED technology to create a homogeneous light patch without
emitting any infrared rays.
Light intensity shall be adjustable at least between 5%-100% and at least 10 different
levels.
Control panel should be equipped in the light head as standard configuration
The maximum movement angle of the spring arm shall be at least up 45°and down 45°.
The thickness of the light head shall be no more than 50mm.
Each LED shall be replaceable individually with the new one to save cost in case of failure,
instead of replacing the module with several LEDs.
TECHNICAL REQUIREMENTS
Central illuminance (lx) ≥ 130,000 lx or better
Light Field Diameter (1m) ≥ 22cm or better
Color Temperature (K) 4,350K or better
Color Rendering Index Ra ≥ 96 or better
Color Rendering Index R9 ≥ 96 or better
Depth of Illumination(L1+L2) (mm) ≥ 1,200mm or better
Dimming Range: 5~100% or better
Radiant energy(average) ≤ 3.6mW/(m2*lx) or better
LED Service Life: ≥ 50,000hrs or better
Max. power consumption of all light sources ≤ 65W or better
Power Supply: 100~240VAC, 50~60Hz or better
Battery Backup built in / Power module supply can support up to 10 hours (normal
state).
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation.

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3.10 OT LIGHT (DOUBLE DOME WITH BUILT IN CAMERA AND RECORDING SYSTEM)
Clinical Specialty Operation Theater
Generic Name OT Light
Clinical Purpose This is ceiling hanged operation theater light used to see and examine
different body parts during surgery to help surgeon to perform surgeries in a
clear visible environment.
S.NO. TECHNICAL SPECIFICATIONS

Double Dome LED type Ceiling OT light


The light shall adopt latest LED technology to create a homogenous light patch
Light intensity shall be adjustable at least between 5%-100% at different levels.
The light shall be with 3 lighting modes for different surgery requirements, including
general lighting mode, full lighting mode and ambient lighting mode for minimally
invasive surgery.
Control pannel Touch screen/Touch pad should be equipped beside the lighthead as
standard configuration for ergonomic user experience.
The light head shall be shape to avoid laminar flow influence by turbulence.
The light shall be mountable to ceiling from a single center. Light head bearing the arms
shall be rotateable 360 degrees around its own axis and mounting point. Each Light
head shall be rotateable at least 300 degrees around its own axis or better
The maximum movement angle of the spring arm shall be at least up 45°and down 50°
or better
The maximum movement range of the horizontal arm & spring arm should be at least
1,600 mm. Or better
The thickness of the light head shall be no more than 50mm or better
Each LED shall be replaceable individually with the new one to save cost in case of
failure, instead of replacing the module with several LEDs as per manufacturer.

TECHNICAL REQUIREMENTS
Specifications Requirements for the Main and Satellite Light
Central illuminance at 1m distance ≥ 160,000 lx or better
Light Field Diameter at 1m distance adjustable from 180~300mm or better
Color Temperature (K) 4,350K or better
Color Rendering Index Ra ≥ 96 or better
Color Rendering Index R9 ≥ 97 or better
Depth of Illumination ≥ 1,000mm or better
Dimming Range: 5~100% or better
Radiant energy(Ee/Ec (average)) ≤ 3.6mW/(m2*lx) or better
LED Service Life: ≥ 50,000hrs or more
Power Supply: 100~240VAC, 50~60Hz

Digital video recorder of OT Light:


Supporting external USB storage device
Default with camera control function
Supporting video recording from other medical devices source

Light Camera to be Fixed in one Dome of Light:


The camera system integrated with the surgical lights also provides a platform for

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medical research purpose, teaching communication and video documenting.


Two Mega Pixels HD (1920×1080 pixels) Camera
26” inches or better Medical grade LED on third arm should be provided
Supporting HDMI/YPbPr/HD-SDI/DVI-D/VGA input signal,
Video output: Component / YPbPr /DVI /VGA

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.11 OPERATION THEATER LIGHT (DOUBLE DOME)


Clinical Specialty Operation Theater

Generic Name Operation Table

Clinical Purpose This is ceiling hanged operation theater light used to see and examine
different body parts during surgery to help surgeon to perform
surgeries in a clear visible environment.

S.NO. TECHNICAL SPECIFICATIONS

Double Dome LED type Ceiling OT light


The light shall adopt latest LED technology to create a homogenous light patch
Light intensity shall be adjustable at least between 5%-100% at different levels.
The light shall be with 3 lighting modes for different surgery requirements, including
general lighting mode, full lighting mode and ambient lighting mode for minimally
invasive surgery.

Control pannel Touch screen should be equipped beside the lighthead as standard
configuration for ergonomic user experience.
The light head shall be shape to avoid laminar flow influence by turbulence, with
Verified Certificate Din-1946 Part 4.
The light shall be mountable to ceiling from a single center. Light head bearing the arms
shall be rotateable 360 degrees around its own axis and mounting point. Each Light
head shall be rotatable at least 300 degrees around its own axis or better
The maximum movement angle of the spring arm shall be at least up 45°and down 50°
or better

The maximum movement range of the horizontal arm & spring arm should be at least
1,600 mm. Or better
The thickness of the light head shall be no more than 50mm or better
Each LED shall be replaceable individually with the new one to save cost in case of
failure, instead of replacing the module with several LEDs

TECHNICAL REQUIREMENTS

Specifications Requirements for the Main and Satellite Light


Central illuminance at 1m distance ≥ 160,000 lx or better
Light Field Diameter at 1m distance adjustable from 180~300mm or better
Color Temperature (K) 4,350K or better
Color Rendering Index Ra ≥ 96 or better
Color Rendering Index R9 ≥ 97 or better
Depth of Illumination ≥ 1,200mm or better
Dimming Range: 5~100% or better
Radiant energy(Ee/Ec (average)) ≤ 3.6mW/(m2*lx) or better
LED Service Life: ≥ 60,000hrs or more
Power Supply: 100~240VAC, 50~60Hz

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NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.12 ANESTHESIA WORKSTATION

Clinical Specialty Operation Theater


Generic Name Anesthesia Machine
Clinical Purpose Anesthesia machine is used mostly in operation rooms to introduce
anesthetic agents inside the body.
S.NO. TECHNICAL SPECIFICATIONS
1
Anesthesia Machine with Ventilator and Modular Patient Monitor
•3 Gas System having O2,N2O and air
•Machine having three or more drawers
•Pin index Cylinder yokes for O2 and N2O
•Pipeline and Cylinder Gauges for O2 ,N2O and Air
•Central gas driven Unit, fresh gas outlet and O2 flush control (35-50L/min or
better)
•4 Antistatic castors, with brake system
•Monitor Shelf
•Electronic Display and Mechanical Controlled Flow Meter O2, N2O and Air with
hypoxic guard with no less than 25% O2 concentration
•O2: 0 to 15 Liters/Minute or better
•N2O: 0 to 10 Liters/Minute or better
•Air: 0 to 15 Liters/Minute or better
•Auxiliary O2 and Air outlet
•1500ml or better Absorber capacity, fully Autoclavable, including Bag/Vent
Switch, CO2 bypass and Manometer Gauge. Complete with mounting Bracket.
Absorber detachable (reusable) including Fresh Gas Hose.
•Vacuum suction along with jar on machine
•Anesthesia machine should be Modular design and Modules can be swapped in
both Anesthesia and Monitor.
 BIS and NMT monitor shall be present alongwith anesthesia machine.
•Heated Breathing System
•Electronic Fresh gas Display
•2 stage adjustable LED Light
•Slectatec backbar with interlocking function for minimum two vaporizers or more
•02 Vaporizer: Isoflurane & Sevoflurane (Supplied by same Manufacturer)
•Four Electrical outlet sockets or more
•The unit should include Active / Passive anesthesia Gas Scavenging system
•Independent ACGO Function
•Emergency Oxygen cylinder for backup on machine

Built-in Anesthesia Ventilator:


•Advanced Anesthesia Ventilator with Adult, Child and Neonatal capability
•Electronic / Microprocessor Controlled and Pneumatically driven
•Display: Large 15” or better full color TFT/LCD Display, Touch –Screen display
parameters, all settings and Alarm Parameters with Back-up touch pad.

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Ventilation Modes:
•Manual/ Spontaneous Ventilation
•Volume Control VCV (IPPV/mode)
• Pressure Control PCV with volume guarantee or equivalent
•SIMV Volume Control + SIMV Pressure Control
•Pressure Support with Apnea
•Cardiac Bypass Mode

Ventilation Monitoring:
•Fio2
•Inspired and Expired Volume
•Monitor Interface Capability
•Spirometer Loops
•PAW, Pressure Waveform, Flow Waveform
•Inverse I:E 4:1 - 1:8 or better
•Gas Specific input connector (Oxygen) ISO standard
•Tidal Volume: 20 to 1500ml or better
•BPM Rate: 4 to 100 bpm or better
•PEEP: off, 3 to 30mH20 or better
•Pressure Inspired: 05 to 70cmH2O or better
•Pressure Limit: 10 to 100cmH20 or better
•Pressure Support Range: 05 to 50cmH20 or better
Power Supply: 220V/50HZ AC
Battery Backup: Minimum 2 Hours or better

User Set Alarm:


•Air Pressure High
•Air Pressure Low
•MV High
•MV Low
•High Oxygen
•Low Oxygen
Static Alarms
•Apnea
•Power Fail
•Battery Low
Supplied Complete with Hose and Power Cable

Multi Gas Monitoring Module for Anesthesia Workstation


•Side-stream measurements with accessories such as sampling line and water trap.
•Method: Infrared / Absorption Gases: Agent Halothane, Isoflurane, Enflurane,
Sevoflurane and Desflurane CO2, N2O and O2
•Automatic Anesthesia Agent Identification display
•User selectable Alarm limits

Vital Sign Monitor Attached with Anesthesia Machine


•Monitor should be Modular support with ETCO2, IBP and Basic function support
ECG. NIBP, TEMP, RESP, HR, SPO2, ST Analysis built in.
•At least 7 parameter Anesthesia Patient monitor
•It should have 15” or more TFT LCD touch display with 12 waveforms or better.

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•It should have following as standard configuration: ECG, HR, RESP, NIBP, SPO2
and TEMP, ST analysis, ETCO2, 2xIBP Diathermy/electro surgical protection.
•Should have alarms for warnings
•Trend: Store and review 48 hours or more

Standard Accessories Adult & Paeds:


•5 Lead patient cable ECG, Software for both 3 & 5 lead monitoring
•SPO2 connecting cable
•SPO2 Reusable finger sensor for adult, pediatric and neonate each
•NIBP connecting Hose with cuff for adult, pediatric and neonate each
•Temperature probe peripheral
•Main cable
•ETCO2 Accessory
•Instruction manual
•2 IBP cable for IBP monitoring with 5 disposable domes
Battery:
•Operating time under the normal use and full change: 04 hours or more
Power supply:
•Power Voltage: 220V-240V 50/60 Hz
•Battery backup 90mins or more
•Monitor, Vaporizer must be supplied from same manufacture as of Anesthesia
Main Unit

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in
case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.13. ELECTRO SURGICAL UNIT/DIATHERMY

Clinical Specialty Operation Theater


Generic Name Electro Surgery Unit/Cautery Machine/Diathermy Machine
Clinical Purpose This machine is used in operation room for cutting and then coagulation
of soft tissues during surgery.
TECHNICAL SPECIFICATIONS
Microprocessor controlled
Digital Error Detection: Human Error or Internal Device error should be displayed on
display
10 Users program settings: 10 different users can store their desired settings which can
easily be accessible any time.
Digital Volume Control
Option for Connects with Smoke evacuator
Percentage output digital display shows on front panel
Automatic bipolar output without using footswitch
Multi mono polar outlets, two hand control outlets and one Laparoscope outlet
With bipolar output power profile to provide good resolution to permit small changes in
power levels for delicate work
Spray Coagulation for the Trans Urethral Resection (T. U. R) and Endoscopic procedures in
urology
Adaptive Return Electrodes Monitoring: With REM facility and alarm should enable in case
of nonpolar output disables.
PURE CUT
BLEND (1), BLEND (2), BLEND (3)
COAG1 (spray), COAG2 (Standard) and AUTO BIPOLAR, FOOT SWITCH BIPOLAR
Technical Specifications:
Output Power
PURECUT 400W at300Ω or better
BLEND1 300W at300Ω or better
BLEND2 250W at300Ω or better
BLEND3 200W at300Ω or better
STANDARD COAG 120Wat 500Ω or better
SPRAYCOAG 70W at 500Ω or better
BIPOLAR CUT 80W at100Ω or better
BIPOLAR COAG 80W at100Ω or better
Operating Frequency: 400KHZ+10% or better
Input Voltage: 220V, 50Hz or better
Input Working Voltage AC180-AC240 volts or better
Input Line Frequency Range 47HZ-63HZ or better
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and vailidation of the equipment .

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3.14 HIGH SPEED ELECTRIC DRILL FOR SPINE SURGERY


Clinical
Orthopedic, OTs
Specialty
Generic
High Speed Electric Drill
Name
Clinical Bone drilling is a universal surgical method generally employed in internal fracture
Purpose fixation, install implants, or to carryout reconstructive surgery. The main purpose of
bone drilling is to produce holes for fixing screws, wires and plates to fasten the
fractured parts for immobilization.
TECHNICAL SPECIFICATIONS
 Control unit with LCD-Display
 Micro motor’s sockets, built-in irrigation pump, socket for foot control
 Electronic motor , 80´000 rpm, with cable 3 m, autoclavable,
 Foot control, electronic, suitable for operating theatre
 Tubing set, sterile, 3 m, 1 x Bottle holder
 Power cord, 1x Lubrication oil spray
 Angled High-Speed surgical handpiece 1:1, FG shank Ø 2,35 mm, L=95mm,
80,000rpm
 Angled High-Speed surgical handpiece 1:1, FG shank Ø 2,35 mm, L=125mm ,
80,000rpm
 Straight High-speed surgical handpiece 1:1, FG shank Ø 2,35 mm, L=95mm,
80,000rpm
 Straight High-speed surgical handpiece 1:1, FG shank Ø 2,35 mm, L=125mm,
80,000rpm Carbide burr length 95mm different sizes Diamond burr length
95mm different sizes
 Carbide burr length 125mm different sizes
 Diamond burr length 125mm different sizes
 Angled hand piece for endoscopic spine surgery with 1:1 transmission and
quick lock system.
 Support sleeve open working length 355 mm dia 4.0 mm
 Support sleeve with distal protector working length 355 mm dia 4.0 mm
 Support sleeve with bevelled protector working length 355 mm dia 4.0 mm
 Carbide milling cutter, round 3.0 mm shaft length 355 mm
 Diamond milling cutter, round 3.0 mm shaft length 355 mm
 Carbide milling cutter, round 3.5 mm shaft length 355 mm
 Diamond milling cutter, round 4.0 mm shaft length 355 mm
 Sterilization case with silicone mate
 Moveable trolley
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in
case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along with
the supply of equipment, which will include calibration and validation of the
equipment.

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3.15 JACKSON TABLE


Clinical
Spine Surgery
Specialty
Generic
Jackson Table, Spine Table
Name
Clinical This table is suitable for spine, combined spine surgery, cervical, thoracic and lumbar spine operations;
Purpose suitable for orthopedic robotic surgery: pelvis, upper limb surgical neck, femoral neck, femoral tuberosity,
lower limb osteotomy and other operations. Cooperate with the robotic system, orthopedic navigation
system and various surgical X-ray machines (C-arm, G-arm, O-arm), intraoperative CT machine and other
surgeries, which can meet the needs of robotic-guided orthopedic trauma surgery and spine surgery.

TECHNICAL SPECIFICATIONS
 It adopts double-column design, the bed frame is made of high-strength carbon fiber material, which
forms a stable, safe and reliable spine operating table with the columns on both sides.
 The carbon surgical bed adopts imported motor, stable, safe and noise-free.
 This carbon operating table can be turned over manually 360°, full perspective without dead angle,
and meet the surgical position requirements from prone position to supine position during surgery.
 The all carbon fiber four-point spine support body is made of Radiolucent material, and there is no
metal to facilitate the shooting of C-arm, G-arm and O-arm without shadows.
 The front and rear adjustment range of the four-point support body is ≥ 1000mm, and the
left and right adjustment range as per manufacturer. Suitable for children and adults.
 The length of the bed is ≥ 2260mm, the width of the base is ≥ 780mm, the length of the bed
is ≥ 2960mm, the width is ≥ 500mm, the lifting range: minimum ≤ 680mm, maximum ≥
1130mm, the table can also be mechanically adjusted in height from 0-400mm, electric
front and rear tilt angle ≥12°, left and right tilt ≥20°.to be quoted from OEM.
 The height of the headrest in prone position can be adjusted from 0-300mm, the headrest can be
adjusted 360° in all directions, and it is equipped with an intubation channel and an intubation
reflector for medical staff, which is convenient for checking whether the intubation is normal.
 The base adopts four-point/Central caster brake to ensure the safety and stability of the table.
 The carbon operating table is detachable, and the base can be retracted and stored for easy
transportation.

Standard configuration
 Spine operating table main body (double column) 1 set
 Carbon frame 1set
 The head positioning system includes a set of head pads (including a special holder)
 Two multi-joint arm supports (including special grippers)
 5. Four-point pads (including high-grade blue sponge pads) 1 set
 Handheld remote control 1pc

NOTE:
The system should be FDA/CE/JIS/MHLW approved.
03 years with parts and services comprehensive warranty.
Life span of the quoted model should be clearly defined by the manufacturer.
Technical training as well as operational training must be provided by the supplier in case if required.
Service manual as well as operational manual must be provided along with the machine.
PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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3.16 CAVITRON ULTRASONIC SURGICAL ASPIRATOR (CUSA)


Clinical
General Surgery, Neuro-Surgery, OT
Specialty
Generic
Ultrasonic Surgical Aspirator
Name
Clinical Cavitron ultrasonic surgical aspirator (CUSA) or simply surgical aspirator is a device originally
Purpose used mainly for hepatic parenchyma resection in the gastrointestinal surgical field. Tissue is
selectively fragmented by an ultrasonically vibrating chip at the tip of the device.
TECHNICAL SPECIFICATIONS
 Ultrasonic Surgical Aspirator for use in different Gastrointestinal Organ, Liver, General,
brain , Laparoscopic & wound care operations
 System should be capable of dual frequency i.e. 25 and 35 KHz.
 Electric ultrasonic aspirating system should have 100 watt output power or more.
 Irrigation flow max. 0~140 ml/min or more.
 Suction pressure 0-0.9 bar or better.
 Steam autoclavable hand piece.
 Ultrasonic surgical aspirator system on mobile trolley with 04 wheel castor.
 Variable energy and control aspiration.
 Integrated suction and irrigation facility.
 Compatible module for electrosurgical module.
 Inclosing of the following accessories and hand piece of :
 One console
 Ultrasonic surgical aspirator with foot switches control system.
 One Piezo electric hand piece angled with resonance frequency 35 KHz or more.
 One Piezo electric hand piece, angled with resonance frequency 25 KHz or more.
 Laproscopic Tip - 5 nos.
 Micro Tips - 5 nos.
 Macro Tips - 5 nos.
 One Autoclaveable hand piece for deep wound
 One Autoclaveable hand piece for superficial wound
 Biopsy collection trap – 10pcs
 Tubing kit for irrigation & Suction - 20 pcs
 Reusable Tip Torque
Technically Mandatory, Financially optional
 One hand piece Angled with resonance Frequency 35 kHZ with 4 pcs of Macro & Micro
TIPS
 Ultrasonic bone cutting hand piece with 4 pcs of long & short TIPS
 Must be compatible for quoted Ultrasonic Surgical Aspirator
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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3.17 FESS INSTRUMENTS SET WITH HIGH DEFINITION ENDOVISION SYSTEM

Clinical
ENT
Specialty
Generic FESS System
Name
Clinical Functional Endoscopic Sinus Surgery (FESS) is one of the most common surgical methods
Purpose to treat chronic sinus infections. In a FESS procedure, the surgeon uses a magnifying endoscope
to see and remove affected tissue and bone.
TECHNICAL SPECIFICATIONS
 ENT Telescope, diameter 4 mm, length 18 cm, autoclavable, variable direction of view
from 15° - 90°, adjustment knob for
 selecting the desired direction of view, fiber optic light transmission incorporated, color
code: gold
 Straight Forward Telescope 0°, enlarged view, diameter 4 mm, length 18 cm,
autoclavable, fiber optic light transmission
 incorporated, color code: green
 Forward-Oblique Telescope 30°, enlarged view, diameter 4 mm, length 18 cm,
autoclavable, fiber optic light transmission
 incorporated, color code: red
 Lateral Telescope 70°, enlarged view, diameter 4 mm, length 18 cm, autoclavable, Fiber
optic light transmission incorporated, Color
 code: yellow
 Forward-Oblique Telescope 45°, enlarged view, diameter 4 mm, length 18 cm,
autoclavable, Fiber optic light transmission
 incorporated, Color code: black
 ENT Shaver system with color display, touch screen, two motor outputs, integrated
irrigation pump and integrated module

Consisting of :
 ENT Shaver Unit
 Mains Cord
 Irrigator Rod
 Two-Pedal Footswitch, two-stage, with proportional function
 Silicone Tubing Set, for irrigation, sterilizable
 Clip Set, for use with Tubing Set
 Connecting Cable, length 100 cm
 Single Use Tubing Set, sterile, package of 3
 Shaver Handpiece
 Suction Shaver Blade with integrated irrigation, Handpiece straight, sterilizable, concave
cutting edge, oval cutting
 window, diameter 4 mm, length 12 cm, color code: blue-green, for use with Handpieces
 Suction Shaver Blade with integrated irrigation, Handpiece straight, sterilizable, serrated
cutting edge, rectangular
 cutting window, diameter 3 mm, length 12 cm, color code: blue-red for use with
Handpieces
 Suction Shaver Blade with integrated irrigation for Handpiece, curved 40°, sterilizable,
cutting edge serrated backwards, double
 serrated, rectangular cutting window, diameter 4 mm, length 12 cm, color code: blue-
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yellow for use with handpieces


 High-Performance Micro Motor, for use with Connecting Cable
 Connecting Cable, to connect High-Performance Micro Motor
 Drill Handpiece, angled, length 12 cm or better, transmission 1:1 (40,000 rpm or more),
for use with high-performance EC micro motor and
 straight shaft burrs
 Drill Handpiece, straight, length 11 cm, transmission 1:1 (40,000 rpm), for use with high-
performance EC micro motor and
 straight shaft burrs
 Tungsten Carbide Shaft Burrs, stainless, different sizes, length 7 cm or better, set of 15
 Nasal Forceps, straight, size 1, with cleaning connector, working length 13 cm
 Nasal Forceps, 45° upturned, size 1, with cleaning connector, working length 13 cm
 Nasal Forceps, straight, through-cutting, tissue-sparing, shape, size 0, width 3 mm, with
cleaning connector, working length 13 cm
 Antrum Grasping Forceps, jaws curved downwards, fixed jaw curved 90°, movable jaw
backward opening 120°, with cleaning
 connector, working length 10 cm
 Antrum Grasping Forceps, jaws curved to right, fixed jaw curved 90°, movable jaw
backward opening 120°, with cleaning
 connector, working length 10 cm
 Nasal Forceps, straight, size 2, with cleaning connector, working length 13 cm

 Bipolar Suction Forceps, 45° upturned, with suction channel, for bipolar coagulation in
paranasal areas, working length 12.5 cm, for
 use with Bipolar High Frequency Cords
 Bipolar High Frequency Cord with two 2 mm cable sockets for Bipolar Suction Forceps
length 450 cm
 Punch, circular cutting, for sphenoid, ethmoid and choanal atresia, diameter 3.5 mm, with
cleaning connector, working length 18
 cm, including Cleaning Tool
 Punch, 45° upturned, punch head diameter 4.5 mm, circular cutting, with cleaning
connector, working length 13 cm
 Frontal Ostium Seeker, double ended, No. 4, both sides curved 90°, tips bent right and
left, length 22 cm
 Antrum Cannula, LUER-Lock, short curved, outer diameter 2.5 mm, length 12.5 cm
 Suction Tube, with mandrel and cut-off hole, with distance marking at 5 - 9 cm, 9 Fr.,
working length 10 cm
 Sickle Knife, pointed, length 19 cm
 Elevator, double-ended, semisharp and blunt, length 20 cm
 HD module, for use with up to 3 link modules, resolution 1920 x 1080 pixels, with
integrated and digital Image Processing Module,

Consisting of:
 Mains Cord, length 300 cm
 DVI-D Connecting Cable, length 300 cm
 Connecting Cable, length 100 cm
 USB Flash Drive,
 USB Silicone Keyboard, with touchpad, US

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 HD link module, for use with FULL HD threechip camera heads, power supply 100 - 120
VAC/200 - 240 VAC, 50/60 Hz

 Three-Chip FULL HD Camera Head, HD compatible, progressive scan, soakable, gas- and
plasma-sterilizable, with integrated
 Parfocal Zoom Lens, focal length f = 15 - 31 mm (2x), 2 freely programmable camera head
buttons
 LED 150, High-Performance LED Light Source with one light outlet, power supply 100 -
240 VAC, 50/60 Hz

 Fiber Optic Light Cable, with straight connector, diameter 4.8 mm, length 300 cm
 27" or more FULL HD Monitor, color systems PAL/NTSC, max. screen resolution 1920 x
1080, image
 format 16:9, Interface: RS 232, power supply 85 - 264 VAC, 50/60 Hz, wall mount with
VESA 100 adaptor

 External 24 VDC Power Supply Mains Cord


 Trolley Powder Coated Rides on 4 antistatic dual wheels,2 equipped with locking (front)
2 fixed shelves, 1 drawer
 uint with lock, (local Supply)

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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S. No. 4 (Critical Care and ICU Equipment)


4.1 MOTORIZED PATIENT BEDS

Clinical
ICU, HDU
Specialty
Generic
Motorized Patient Beds/Electro-Hydraulic Patient Beds
Name
Clinical A full electric hospital bed for home use features electric motor controls that raise the head, foot
Purpose and height of the bed frame with a push of a button. ... These full electric hospital beds allow
patients to dial in their desired bed height without the aid of a caretaker, making transfers to and
from a bed easier.

TECHNICAL SPECIFICATIONS
4 motors
Electronic adjustments of backrest, footrest, height
Trendelenburg and Reverse Trendelenburg functions
Fowler, Vascular and Cardiac positions
Auto-contour
Function-Lock System to prevent unauthorized use
Angle indicator for backrest adjustment and
Trendelenburg positions
Auto-regression system
Electronic CPR
Auto-CPR button + manual
Lockable and fold-away PP side rails
Lockable and detachable Polypropylene head and foot boards
4 section, detachable mattress platform
Electrostatic powder coated metal frame
Gradually adjustable footrest
Drainage bag hooks at both sides
IV pole sockets located at four corners
Protective plastic corner bumpers
Central lockable castors
Height adjustable stainless steel IV pole

Electrical and Technical Data


Power 200-240VAC, 1.5A max, 50-60 Hz
Electrical shock protection, Class 1, Type B
Liquid ingress protection, IPX4-IP66
Battery backup
Overall length 210cm or better
Overall width 99 cm or better
Height Range 35-75cm or better
Trendelenburg 0-150 or better
Reverse Trendelenburg 0-150 or better
Back rest angle maximum 700 or better
Leg rest angle maximum 350 or better

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Caster diameter 15cm or better


Safe working load 250 Kg or more
Stainless steel IV Pole
Oxygen bottle holder

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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4.2 HIGH END ECHO-CARDIOGRAPHY MACHINE WITH TEE PROBE


Clinical
Cardiology
Specialty
Generic
ECHO Machine
Name
Clinical An echocardiogram uses electrodes to check your heart rhythm and ultrasound technology to
Purpose see how blood moves through your heart. An echocardiogram can help your doctor diagnose
heart conditions. An echocardiogram uses sound waves to produce images of your heart.
TECHNICAL SPECIFICATIONS
The system must be latest generation, highest end & technologically advanced Digital 4D (Live
3D) echocardiography system
System must be offered with a minimum of 5,00,000 (5 Million) digital processed channels.
Original technical data sheet should be enclosed in technical bid to support the number of
channels on the system. If not mentioned, the technical bid will not be accepted.
System must have adult cardiology transducer with either single crystal technology or pure
wave technology or matrix or broad band for excellent gray scale image quality on difficult to
image patients. Please mention the technology used in the transducer. Original technical data
sheet should be enclosed in technical bid to support the crystal technology
System must be offered with a minimum 21 inches or more high-resolution flat panel medical
grade display monitor with nearly infinite position adjustments. Company should provide
wider monitor if available
System should have at least four (04) imaging universal active probe ports with electronic
switching facility from keyboard without probe adapter
System should be capable of supporting second-generation 4D (Live 3D) matrix transducer
capable of supporting matrix exceptional 4D (Live 3D) echo, 4D (Live 3D zoom) and operating
modes must include B, 2D M-Mode, PW, Spectral Doppler, Color Doppler, THI and TDI.
Image storing facility on in built hard disc or MOD/CD/DV-RW facility should be available. In
built- in hard disk the capacity should be of minimum 500GB or more. System should have
extensive image management capability including thumbnail review, cine loop editing etc.
System must be offered with Speckle reduction imaging: Image processing technique to
remove speckles and clutter artifacts. Application for Cardiac, Peripheral, Pediatric, adult
should be available
System should have 4D (Live 3D) echocardiography capabilities with color flow imaging
System should be capable of scanning depth of 30cm. scanning depth should be clearly
mentioned in the technical quote if not mentioned please attach a letter from the
manufacturer along with the technical bid clearly stating the scanning depth of 30cm in the
offered system.
Should be able to perform advanced quantification measurements like strain & strain rate
quantification
Frame rate with 2000 FPS or more in 2D Mode
Fully automated 4D volume (Live 3D) calculation for RV
Volume per second should be 400 Mega Voxel/s or better
The system should have the facility of displaying the three planes of the 3D data set.
Integrated stress echo facility to perform stress echo exams.
The system should be offered with user-friendly high-resolution user interface touch panel of
12 or more inches or intuitive keyboard.

The following Probes should be quoted with the main equipment:

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1. Adult Phase array Probe with 4D Probe was added.


2. TTE Probe for Adult and paeds to be quoted as Optional.
3. Paeds Phase Array Probe
4. TEE Probe for Adult and paeds

DICOM Basic
Digital Thermal Printer
Online UPS Pure Sine-Wave 3KVA or more

NOTE:
5. The system should be FDA/CE/JIS/MHLW approved.
6. 03 years with parts and services comprehensive warranty.
7. Life span of the quoted model should be clearly defined by the manufacturer.
8. Technical training as well as operational training must be provided by the supplier in
case if required.
9. Service manual as well as operational manual must be provided along with the
machine.
10. PPM Schedule should be share with Biomedical Engineering Department along with
the supply of equipment, which will include calibration and validation of the
equipment.

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4.3: PORTABLE BRONCHOSCOPE

Clinical
ICU, Pulmonology ENT
Specialty

Generic Name Portable Bronchoscope

A single use disposable bronchoscope has significant advantages related to


Clinical reducing the risk of cross infection, ease of compliance with cleanin and
Purpose disinfection regulations during non-working hours, and reducing costs related to
trauma repairs during use or reporcessing of the equipment.

TECHNICAL SPECIFICATIONS
Full High Definition Video Processor & Light Source

Brilliant, Full high definition (1920 x1080 HD images for a clear and more
detalied visualization.
It should be HD Digital/optical Video and image processor.

Chromo -endoscopy technology combined with optical / digital image


processing. It provides a clear and bright image contrast that allows a better
vision of mucosa and blood vessels in the GI tract.
Zoom upto 2X or better.
white Balance Adjuster, USB Ports, image enhancement, freeze scan &
integrated or separated video recorder with 500GB storage capability or better

Patient data management software from same manufacturer or better.


Outputs: HD-SDI, DVI, VGA, S-Video & CVBS
Light source (Integrated/Separated):
Main Lamp Xenon life span: 500 hrs or better
Auxiliary lamp LED/Halogen should be available.
HD Medical Grade Monitor:
HD Medical Grade Monitor:
26" Medical Grade or better
Aspect ratio of 16:9 or better
With all standard accessories
High Definition Bronchoscope:
HIgh Definition Broncho video scope with advanced technologies features.
Outer diameter 5.7mm or better
Angle of view 120◦ or better
Focal range 2-100mm or better
Instrument channel 2.0mm or better
Working length 600mm or better
Wide range 4-way angulations: or better

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Up 180◦
Down 130◦
with standard set of accessories
Endoscopic Cart/Troley (From the Manufacturer)
Compatible with above Endoscopes/system
Erosion free durable material
Should have castors wit brakes.
Endoscopic storage cabinet (Supplied Locally):
Compatible with above Endoscopes
Front opening / with complete fitting
Should havecapability to store 5 endoscopes
Endoscopic disinfector (Supplied Locally):
Automatic disinfectin system& Should be able to clean all external/internal
surfaced of endoscopes.
Compatible with quoted endoscopes.
Note:
The system should be FDA/CE/JIS/MHLW approved.
03 years with parts and services comprehensive warranty.
Life span of the quote model should be clearly defined by the manufacturer.
Technical training as well as operational training must be provided by the
supplier in case if required
Service manual as well as operational manual must be provided along with the
machine.
PPM schedule should be share with Biomedical Engineering Deptt: along with
the supply of equipment, which will include calibration and validation of the
equipment.

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4.4 PORTABLE DOPPLER ULTRASOUND


Clinical
ICU, HDU, Emergency
Specialty
Generic
Portable Ultrasound Machine
Name
Clinical Portable ultrasound machines provide the flexibility and mobility to travel with clinicians and
Purpose image patients where they are in real-time. Portable ultrasound machines empower clinicians
to obtain high-quality images without relying on a single machine's availability.
TECHNICAL SPECIFICATIONS
15 inch full touch screen
Seamless touch screen without keys and knobs ensures easy cleaning
Touch screen supports operation with gloves on
10 seconds or better screen locking feature for easy cleaning the screen anytime
during the exams
Three Active transducer connectors on the main unit for Trans-Thoracic Probes
Three transducers can work under battery supply
Continuously track the color flow and automatically adjust the Color box position and
angle in real time scanning for fast and simple vascular exams
128 GB or more SSD
Built-in battery which can support at least 1 hours or more scanning
290mm or better range height adjustable Compact Original trolley with retractable
power cable assures tidiness and safeness for transport and storage
3 seconds or better boot up from standby with one touch on the screen
Offers direct and fast way to enter and exit full screen image zooming by touch gesture
Max. Depth Display 30 cm or more (probe dependent)
Prospective cine saving for 450 s or better
Convex probe 1.5-6.0 MHz or better
Linear probe 4.0–12 MHz or better
Adult Phased Array probe 1.5–4.0 MHz or better
Dedicated Software for support of Needle Visualization Enhancement
Optional (Should be quoted Separately):
Micro-Convex Probe 3.0–10 MHz or better
TEE Probe 2.0-7.0 MHz or better
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the
supplier in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of
the equipment.

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4.5 .A: DEFIBRILLATOR (360 JOULES)


Clinical
ICU, HDU, Emergency
Specialty
Generic
Defibrillator
Name
Clinical A defibrillator is a device that gives a high energy electric shock to the heart
Purpose of someone who is in cardiac arrest. This high energy shock is called
defibrillation, and it's an essential part in trying to save the life of someone
who's in cardiac arrest.
TECHNICAL SPECIFICATIONS
Semi-automatic maximum 360 joules biphasic defibrillator with monitor and AED
mode.
Synchronized output with ECG.
Control of energy charging/ delivering on main panel and paddle.
The energy range should be adjustable for Paeds and adults up to 360Joules.
Charging Time for full energy will be less than 08 sec.
Screen Size of approx. 6.5 inch or better colored.
Display of HR Adult: 15 to 300 bpm, Pediatric, Neonate: 15 to 350 bpm
ECG through Pads / paddles and 3 Lead ECG patient cable with arrhythmia
detection
Built in recorder for printing of full summery on standard paper including
waveforms, Frozen Waveforms, Event Summary, Tabular Trends, User test, and
Configuration.
Alarms for High and low Heart rate, low battery warning.
AC 220V / 50 Hz operated.
Built-in Rechargeable battery with charger for at least 80 shocks at max. Energy
and 2.5 hours or better, Monitoring
Auto tester/self-check.
External pediatric and adults Paddles, ECG cable with reusable electrodes for adult
& Paeds.
AED facility.
Pacing rate:30-210ppm
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier
in case if required.
 Service manual as well as operational manual must be provided along with the
machine.
 PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of the
equipment.

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4.5 .B: DEFIBRILLATOR (200 JOULES)

TECHNICAL SPECIFICATIONS

Semi-automatic maximum 200 joules biphasic defibrillator with monitor and AED mode.
Synchronized output with ECG.
Control of energy charging/ delivering on main panel and paddle.
The energy range should be adjustable for Paeds and adults up to 200Joules.
Charging Time for full energy will be less than 08 sec.
Screen Size of approx. 6.5 inch or better colored.
Display of HR Adult: 15 to 300 bpm, Pediatric, Neonate: 15 to 350 bpm
ECG through Pads / paddles and 3 Lead ECG patient cable with arrhythmia detection
Built in recorder for printing of full summery on standard paper including waveforms, Frozen
Waveforms, Event Summary, Tabular Trends, User test, and Configuration.
Alarms for High and low Heart rate, low battery warning.
AC 220V / 50 Hz operated.
Built-in Rechargeable battery with charger for at least 80 shocks at max. Energy and 2.5 hours
or better, Monitoring
Auto tester/self-check.
External pediatric and adults Paddles, ECG cable with reusable electrodes for adult & Paeds.
AED facility.
Pacing rate:30-210ppm

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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4.6 PORTABLE VENTILATOR

Clinical Specialty ICU, HDU, Emergency


Generic Name Portable Ventilator/Transport Ventilator
Clinical Purpose Transport ventilators provide ventilator support for patients who cannot
breathe on their own or who require assistance maintaining adequate
ventilation because of illness, trauma, congenital defects, or the effects of
drugs.
TECHNICAL SPECIFICATIONS

Suitable for adult and pediatric


Electronically controlled turbine/Oxygen technology for supporting
transportation of the patient inside hospital or inside intensive care
unit
Angle adjustable full color 4-inch TFT touch screen or better
Dedicated inspiratory & expiratory flow sensor to ensure the
ventilation accuracy.
Tidal Volume: 50ml – 2000 ml or better
PEEP: Off,1-20cmH2O or better
Respiratory rate: 1-100 bpm or better
Full-automatic system check procedure.
Invasive and non-invasive ventilation which could be used inside ICU
or outside ICU.
Close loop ventilation capacity with basic ventilator modes for invasive
& non-invasive ventilation like V-A/C, P-A/C, V-SIMV, P-SIMV, PSV,
CPAP, Duo level,
Adaptive Minute Ventilation
NIV Mode (Non-Invasive Ventilation)
ATRC (Automatic Tube Resistance Compensation)
Battery backup of up to 180min or better
 40Ft Cylinder shall be quoted.
 Carrying case shall be quoted.
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the
manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided
along with the machine.
 PPM Schedule should be share with Biomedical Engineering
Department along with the supply of equipment, which will include
calibration and validation of the equipment.

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4.7 MECHANICAL VENTILATOR


Clinical
ICU, HDU
Specialty
Generic
Mechanical Ventilator/ICU Ventilator
Name
Clinical A mechanical ventilator is a machine that helps a patient breathe (ventilate) when they are having
Purpose surgery or cannot breathe on their own due to a critical illness. The patient is connected to the
ventilator with a hollow tube (artificial airway) that goes in their mouth and down into their main
airway or trachea.
TECHNICAL SPECIFICATIONS
Suitable for adult, pediatric and neonatal patients (minimum 2kg) or better
Full color 15.6 TFT touch screen with high resolution (1920*1080) or better
Pneumatically driven & electronically controlled ventilator
Full-automatic system check procedure.
Invasive and non-invasive ventilation which could be used inside ICU or outside ICU.
Backup air supply, which could guarantee the ventilator work properly in emergency condition
such as no air supply or no electricity supply.
With real-time gas pressure electronic display.
Dedicated inspiratory & expiratory flow sensor to ensure the ventilation accuracy. Inspiratory &
Expiratory module can be detachable and autoclavable (134◦C).
Modular designed main-stream / side-stream CO2 concentration monitoring measurement.
 Ventilation Mode may vary from manufacturer to manufacturer.
2 Ventilation Modes for invasive & non-invasive
Having the following ventilation modes or similar ones
V-A/C (Volume Assist/Control )
P-A/C (Pressure Assist/Control)
V-SIMV (Volume-Synchronized Intermittent Mandatory Ventilation)
P-SIMV (Pressure-Synchronized Intermittent Mandatory Ventilation)
PSV (Pressure Support Ventilation)
CPAP (Continuous positive airway pressure ventilation)
nCPAP (nasal Continuous positive airway pressure ventilation) quoted as Optional.
Duolevel (Dual Level Positive airway pressure ventilation)
APRV (Airway Pressure Release Ventilation)
PRVC (Pressure Regulated Volume Control)
PRVC-SIMV (PRVC-Synchronized Intermittent Mandatory Ventilation)
VS(Volume support)
Apnea Back-up
AMV (Adaptive minute ventilation)
CPRV (Cardio-pulmonary resuscitation ventilation)

3 Procedures and Decision Support Function


Sigh function
High flow O2 Therapy
Pneumatic Nebulizer
Expiratory Hold
Inspiratory Hold
Manual breath
O2 Enrichment

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Suction support
P0.1 measurement
NIF measurement
PEEPi measurement
Low flow PV tool to decide optimal PEEP setting. Calculate and display upper and lower inflection
points. Store up to 4 historical measurements.
ATRC: automatic tube resistance compensation
Weaning Tool
Recruitment Maneuver: Sustain inflation method.
Basic flow: automatic adjustment, range: 3-40L/min(invasive);10-65L/min(non-invasive)
or better

4 Control Parameters Specification


Tidal Volume: 2-2500ml (neonatal 2-100ml) or better
Respiratory rate: 1-100 breath/min (neonatal 1-150) or better
SIMV rate: 1-60 breath/min or better
I:E ratio: 1:10- 4:1 or better
Inspiratory Time: 0.1-10s or better
Peak Flow:180L/min or better
Inspiratory Pressure: 1-100cmH2O or better
Support Pressure: 0-100cmH2O or better
PEEP: 0-50cmH2O or better
Pressure Trigger: -10- -0.5cmH2O, OFF or better
Flow Trigger: 0.5-20 L/min (neonatal 0.1-5.0L/min), OFF or better
Exp% : Auto, 10-85% or better
FiO2: 21-100% or better

5 Monitored Parameters Specification


Airway Pressure: PEEP, Ppeak, Pplat, Pmean
Minute Volume: MV, MVspn, MVleak
Tidal Volume: TVi, TVe, TVe spn, TVe/IBW
Respiratory Rate: ftot, fmand, fspn
O2 concentration: FiO2
CO2 parameter: EtCO2, V’CO2, Vdaw, slopeCO2, Vdaw, Vdaw/TVe, Vtalv, V’alv, ViCO2, VeCO2
Lung Mechanics: Rinsp, Rexp, Cstat, Cdyn, RCexp
Others: RSBI, NIF, WOB, Tinsp, I:E
Display graphics including standard waveforms showing pressure, flow, volume, CO2, Pleth,
auxiliary pressure over time, show up to 3 waveforms simultaneously
Display Loops including Pressure-Volume, Flow-Volume, Flow-Pressure, show up to 2 loops
simultaneously
Waveforms and loops display simultaneously
Configurable graphical and numerical display
Show trended data for the last 96 hours or better
Store 5000 history log information or better

6. Adjustable Audio and Visual Alarms


Airway Pressure: High/Low
Minute Volume: High/Low
Respiratory Rate: High/Low
Expiratory tidal volume: High/Low

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PEEP: High/Low
Inspired O2 concentration: High/Low
EtCO2: High/Low
Apnea
Breathing circuit disconnect / Leakage
Breathing circuit occlusion
Power Supply Fail
Gas Supply Fail

7. Power and Gas Supply


External AC power supply: 100~240V, 50/60Hz
Integrated Li-Ion backup battery run time: Up to180min or better

8. Communication
Ventilator Data, trends and screenshots can be exported to USB
Communication ports: RS232, VGA, USB, Ethernet, Nurse Call etc.
NOTE:
 The system should be FDA/CE/JIS/MHLW approved. One Certificate mandatory.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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4.8 PATIENT MONITOR


Clinical Specialty ICU, HDU, OT’s etc. General Diagnostics
Generic Name Patient Monitor/Cardiac Monitor/Vital Sign Monitor
Clinical Purpose Patient monitors measure, record, distribute and display combinations of biometric values such as heart rate,
SPO2, blood pressure, temperature and more. High-capability, multi-function monitors are typically used in
hospitals and clinics to ensure a high level of quality patient care.
TECHNICAL SPECIFICATIONS
(5ch ECG, SpO2, NIBP, Dual IBP, TEMP, Resp.,ETCO2)
Display for easy Viewing 15” or better color TFT/LCD/ LED for easy set-up User selective 10 or better traces/ waveform
display.
ECG, SpO2, NIBP, IBP, 2-TEMP, and Respiration EtCO2 (Side stream type with basic accessories)
23 or more Arrhythmias analysis should be detected and alarmed
Multi-lead ECG algorithm
S-T and QT Analysis
Pacemaker detection.
Support heart rate analysis and dynamic NIBP analysis
Save up to 500 or more Event management and 48 hours or more waveforms IBP cable and sensor kit
Up to 72 hours of graphic and tabular trend of all parameters,
PERFORMANCE:
Heart rate: 30 ~ 300 bpm or better on either sides And Ped/Neo:15-350bpm or better
Respiration
Respiration rate: 2~150bpm or better on either side.
SPO2:
Range: 0 ~ 100% or better on either side
Temperature:
Range; 0 -50Cº (32 - 122Fº)
NIBP:
Range: Adult: SYS 25-290mmHg DIA 10-250mmHg Average: 15- 260mmHg
Pediatric: SYS:25-240mmHg DIA:10-200mmHg Average:15- 215mmHg
Neonatal: SYS:25-140mmHg DIA:10-115mmHg Average :15- 125mmHg
Alarm
Alarm: All parameters on/off selective independently
Power input 220Vac,50Hz
With Battery Backup time: Minimum 02 hours or better
ACCESSORIES:
• ECG 5 Lead cable. 1
• Disposable Electrodes Adult, Neonate & Paeds. 20 each
• SPO2 Finger sensor with fixed or detachable extension (each for adult, Peads and neonate) 1
• NIBP Reusable Neonate, Paeds & Adult Cuff 1
• NIBP Hose 1
• AC power code 1
• Operation Manual 1
• ETCO2 (Side stream) with basic acc. 1
• IBP Cable 1
• Temperature sensor & cable 1
NOTE:: The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of equipment,
which will include calibration and validation of the equipment.

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S.NO.5 GENERAL EQUIPMENT & MISCELLANEOUS ITEMS


5.1 PATIENT LIFT SYSTEM
Clinical
OT, ICU, HDU
Specialty
Generic
Patient Lift System/Patient Hoist/Patient Transfer System
Name
Clinical Patient lifts are designed to lift and transfer patients from one place to another (e.g.,
Purpose from bed to bath, OT to ICU, chair to stretcher). These should not be confused with
stairway chair lifts or elevators. Patient lifts may be operated using a power source or
manually.

TECHNICAL SPECIFICATIONS
 Electromotive lifting Controlled by remote.
 Built-in Battery Backup with two batteries for at least 24 hours.
 Optimum solution for supine lifting of patients in critical care.
 For repositioning and turning of parallel and bedridden patients in CCU, ICU
and HDU or Ward.
 For transferring patients on chairs or Toilet seat from bed.
 For transferring patient from shifting trolley to bed or OT table.
 Safe Working load: 180 kg or batter.
 Vertical column for maximum support and accurate positioning
 Powered chaise (Leg extension) for convenient transfer to toilet and Chair
 Battery Discharge indicator.
 Display of total usage time.
 System Failure Override.
 Protection Class: Lifter IPX-4
 Protection Class: Hand Set IPX-7
 Minimum Lifting height: 225 mm or batter.
 Maximum Lifting height: 1540 mm or batter.
Accessories:
 1 x Patient Bar for lifting in Spine position.
 1 x Patient powered bar for lifting in chair position
 6 x Slings for spine and chair position lift.
 Built in Weight Scale (Optional)
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the
manufacturer.
 Technical training as well as operational training must be provided by the
supplier in case if required.
 Service manual as well as operational manual must be provided along
with the machine.
 PPM Schedule should be share with Biomedical Engineering Department
along with the supply of equipment, which will include calibration and
validation of the equipment.

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5.2 ENT EXAMINATION UNIT


Clinical
ENT
Specialty
Generic
ENT Examining Unit
Name
Clinical ENT Examination is consists of multiple equipment used for diagnosis and treatment
Purpose of different diseases of Ear, Nose and Throat.

TECHNICAL SPECIFICATIONS
 ENT Treatment Unit
 Spray : 03 minimum
 Suction : 02 minimum
 Mirror quick heater : 01 minimum
 Ventilation : 01 minimum
 Reflection light with curved pole : 01 at least
 Pen light : 01 at least
 Medicine bottle : 04 minimum
 Deposit for used instrument (100mm Can) : 02 or more
 83mm Can : 03 or more
 53mm Can : 02 or more
 Instrument tray : 01 or more
 Maximum power consumption: 1200VA
 Compressor motor : 2.3kgf/㎠ ± 0.3kgf㎠ or better
 Suction motor : 680mmHg or better

2. Patient Chair
 Hydraulic Mechanism
 Rotation : 340 Deg. Manually or better
 Foot switch for Up / Down / Front / Rear
 Armrest : 360 Deg. Rotation
 Headrest : Up/Down/Front/Rear
 Foot switch : 01
 Power cable : 01
 Power supply: AC 220V, 60Hz
 Power consumption: 460VA
 Hydraulic Mechanism
 Rotation : 340 Deg. Manually or better
 Foot switch for Up / Down / Front / Rear
 Armrest : 360 Deg. Rotation
 Headrest : Up/Down/Front/Rear

3. Endoscope System
 Otoscope : 01 or more
 Power cable : 01 or more
 Video cable : 01 or more

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 Gun type camera head with light guide cable combined : 01 or more
 Adapter lens (F-25mm) : 01 or more
 LCD 19” Monitor with arm : 01 or more
 Foot switch : 01
 Power consumption : 200VA
 Features : 1/2/4 capture or better
 Video output : 3 x CVBS or better
 Image sensor : 1/3” CCD or better
 Aspect ratio : 4:3 or better
 Frame rate : 25/30fps@D1 or better
 Head type : Gun type
 Light source : LED, One channel
 Color temperature : about 5,800K or better
 Lamp life : about 30,000hours or better

4. Doctor Stool
 Main body : 01
 Adjustment : Gas cylinder
 Seat size : 450mm x 390mm or better

NOTE:

The system should be FDA/CE/JIS/MHLW approved.


03 years with parts and services comprehensive warranty.
Life span of the quoted model should be clearly defined by the manufacturer.
Technical training as well as operational training must be provided by the
supplier in case if required.
Service manual as well as operational manual must be provided along with the
machine.
PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of the
equipment.

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5.3 BLOOD WARMER


Clinical
Hematology, ICU, HDU, Emergency
Specialty
Generic
Blood Warmer/Fluid Warmer
Name
Clinical Blood warmers were developed to reduce the risk of hypothermia associated with the
Purpose infusion of cold blood products. During massive transfusion, these devices are used
with compression sleeve, which induce a major stress to red blood cells.

TECHNICAL SPECIFICATIONS
 Delivers blood and intra venous fluid to the patient and normothermic
temperature at wide range of flow rates from gravity flow rates to 10 to 5000
ml/hr.
 Keeps blood/fluid warms between temperature range of 37C to 42C
 Dedicated disposable triple lumen tubing that eliminates patient line cool
down of infuscate
 Single step programming of warmer
 Easy to setup and easy to use
 Simple once a year maintenance
 Displays set point of recirculating reservoir
 Audible and visual alarms if reservoir temperature reaches above the set valve
 Meets all the AABB standards for blood warming
 Must be easy to clean
 Disposable must be latex free
 Should have built in safety audio and visual alarms for check disposables, add
recirculating solution and over temperature
 Built in over temperature test button and alarm test button.

NOTE:

The system should be FDA/CE/JIS/MHLW approved.


03 years with parts and services comprehensive warranty.
Life span of the quoted model should be clearly defined by the manufacturer.
Technical training as well as operational training must be provided by the
supplier in case if required.
Service manual as well as operational manual must be provided along with the
machine.
PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of the
equipment.

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5.4 AIRWAY MANAGEMENT SYSTEM


Clinical
Anesthesia, ICU, HDU
Specialty
Generic
Airway Management System
Name
Clinical The different types of medical devices used to maintain or open an individual's airway
Purpose include the oropharyngeal airway (OPA), nasopharyngeal airway (NPA), and
endotracheal airway (ETA).

TECHNICAL SPECIFICATIONS

Monitor for Endoscopes, Kit, screen size 7" or more with 1280 x 800
1 pixel resolution or better, two camera inputs, a USB and a HDMI
port, optimized user interface,
video and image capturing in real time on SD card, playback of recorded
video clips and still images, data transfer from SD card to USB flash
drive possible, splash-proof according to IP54, suitable for wipe
disinfection, shock-resistant ABS plastic housing,
intelligent power management with rechargeable Li-Ion batteries,
VESA mounting option, power adaptor for EU, UK, USA and Australia,
power supply 110 - 240 VAC, 50/60 Hz,
consisting of:
Monitor
SD Card, 16 GB
Protection Cap
VESA Quick Clip
Power Supply
Plug Adaptor
IEC (ROW) Plug
Adapter Cable

Pocket Monitor Set, unit with LCD monitor and power supply for all
2
video laryngoscopes, with system interface,
screen size 3.5"or more, documentation of images and video sequences
saved on internal memory, monitor movable via
two rotation axes, rechargeable Li-Ion battery, 1 h operation
time, exchangeable battery pack, 2 h charging time,
power management with capacity indicator, protection class IPX8, for use
with Video Laryngoscopes
consisting of:
Pocket Monitor
Battery, rechargeable
USB Data Cable
Protection Cap

Video Laryngoscope MAC #2, technology, with laryngoscope blade, size 2,


3
with system
interface, documentation of images and video sequences via Blue Button,
for use with Connecting Cable for Monitor

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Video Laryngoscope MAC #3, technology, with laryngoscope blade, size 3,


4
with system interface, documentation
of images and video sequences via Blue Button, for use with Connecting
Cable for Monitor
Video Laryngoscope MAC #4, technology, with laryngoscope blade, size 4
5
, with system interface, documentation
of images and video sequences via Blue Button, for use with Connecting
Cable for Monitor
Video Laryngoscope MAC #0, technology, with laryngoscope blade, size 0
6
, with system interface, documentation
of images and video sequences via Blue Button, for use with Connecting
Cable
for Monitor

Video Laryngoscope MAC #3, technology, with laryngoscope blade, size 3,


7
with system interface, documentation
of images and video sequences via Blue Button, with catheter introduction
sizes 14 - 16 Fr., for use with Connecting
Cable for Monitor

Video Laryngoscope MAC #4, technology, with laryngoscope blade, size 4,


8
with system interface,
documentation of images and video sequences via Blue Button, with
catheter introduction sizes 16 - 18 Fr., for use
with Connecting Cable for Monitor

Video Laryngoscope #0, technology, with laryngoscope blade, size 0,


9
with system interface,
documentation of images and video sequences via Blue Button, for use
with Connecting Cable for Monitor

Video Laryngoscope #1, technology, with laryngoscope blade, size 1,


10
with system interface,
documentation of images and video sequences via Blue Button, for use
with Connecting Cable

Video Laryngoscope Set for adults, technology, for difficult intubation,


11
with system interface, documentation of
images and video sequences via Blue Button, with catheter introduction
sizes 16 - 18 Fr., including Guide which is
adapted to shape of the blade
consisting of:
Guide
Video Laryngoscope

Video Laryngoscope for Paeds., pediatric, technology, for difficult intubation


12
in children, with system interface,
documentation of images and video sequences via Blue Button, for use
with Connecting Cable for Monitor

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Imager, with system interface, for manual and machine disinfection up to


13
65 °C and High Level Disinfection (HLD)
acc. to US standards, for use with Connecting Cable Monitor

Video Laryngoscope MAC #4, with laryngoscope blade, size 4, for single
14
use, package of 10,

Video Laryngoscope MAC #3, with laryngoscope blade, size 3, for single
15
use, package of 10,

Flexible Intubation Video Endoscope Set 5.5 x 65 or better, CMOS


16
technology, with suction valve,
deflection up/down 140°/140° or better,
direction of view 0°,
angle of view 100°,
working length 65 cm or better,
total length 94 cm or better,
working channel inner diameter 2.1 mm,
distal tip outer diameter 5.5 mm or better
consisting of:
Flexible Intubation Video Endoscope 5.5 x 65 or better
Case
Pressure Compensation Cap
Leckage Tester
Tube Holder
Cleaning Brush
2x Irrigation Adaptor
Suction Valve

Bronchoscope Insertion Tube, size 4, sterile


Bronchoscope Insertion Tube, size 2, sterile
Plug
Protection Cap

Flexible Intubation Video Endoscope 4 x 65 or better, Set, CMOS


17
technology, with suction valve,
Deflection up/down: 140°/140° or better
Direction of view: 0°
Angle of view: 100°
Working length: 65 cm
Total length: 93 cm
Working channel inner diameter: 1.5 mm
Distal tip outer diameter: 4 mm,
consisting of:
Flexible Intubation Video Endoscope 4 x 65
Leakage Tester
Tube Holder
Irrigation Adaptor
(2x) Suction Valve

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Bronchoscope Insertion Tube, size 4, sterile


Bronchoscope Insertion Tube, size 2, sterile
Plug, black, package of 10
Protection Cap,

18 Flexible Intubation Video Endoscope 3 x 51.5 or better, Set, technology,


deflection up/down 140°/140° or better,
direction of view 0°,
angle of view 100°,
working length 51.5 cm or better,
total length 72 cm or better,
distal tip outer diameter 2.85 mm or better
consisting of:
Flexible Intubation Video Endoscope 3 x 51.5 or better
Leakage Tester
Tube Holder
Bronchoscope Insertion Tube, size 4, sterile
Bronchoscope Insertion Tube, size 2, sterile
Protection Cap

19 Flexible Intubation Video Endoscope 3.5 x 65,


direction of view: 0°,
angle of view: 90°,
working length: 65 cm,
outer diameter: 3.5 mm,
working channel diameter: 1.2 mm,
deflection up/down: 180°/180°,
sterile, for single use, package of 6,

rigid intubation video endoscope with deflectable tip, CMOS technology,


20
with documentation of images and video
sequences via BlueButton, usable with Tube Holderfor tube fixation and
O2 application,
deflection up/down 60°/0°,
direction of view 0°,
angle of view 100°,
working length 41 cm,
total length 60 cm,
distal tip outer diameter 5.5 mm
The following accessories are included in delivery:
Rigid Intubation video endoscope
Leakage Tester
Tube Holder for use with Connecting Cable

21 Video-Rhino-Laryngoscope with Monitor,


direction of view 0°,
angle of view 100°,
deflection up 140, down 140°,

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working length 30 cm,


O.D. 2.9 mm
Following accessories are included:
Video-Rhino-Laryngoscope, 2.9 mm KIT
Monitor for Endoscopes, Kit

22 Intubation Fiberscope 5.2 x 65, eyepiece version, with suction valve,


deflection up/down 140°/140°,
direction of view 0°,
angle of view 120°,
working length 65 cm,
total length 93 cm,
working channel inner diameter 2.3 mm,
distal tip outer diameter 5.2 mm,
consisting of:
Intubation Fiberscope 5.2 x 65
Case
Pressure Compensation Cap
Leakage Tester
LIPP Tube Holder
Cleaning Brush
2x Irrigation Adaptor
Suction Valve
Bronchoscope Insertion Tube, size 4, sterile
Plug for use with LED Battery Light Sources

23 Intubation Fiberscope 3.7 x 65, eyepiece version, with suction valve,


deflection up/down 140°/140°,
direction of view 0°,
angle of view 120°,
working length 65 cm,
total length 93 cm,
working channel inner diameter 1.5 mm,
distal tip outer diameter 3.7 mm,
consisting of:
Intubation Fiberscope 3.7 x 65
Case
Pressure Compensation Cap
Leakage Tester
LIPP Tube Holder
Cleaning Brush
Irrigation Adaptor
Suction Valve
Bronchoscope Insertion Tube, size 4, sterile
Bronchoscope Insertion Tube, size 2, sterile
Plug, for use with: LED Battery Light Sources

24 Intubation Fiberscope 2.8 x 65, eyepiece version, with suction valve,


deflection up/down 140°/140°,

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direction of view 0°,


angle of view 90°,
working length 65 cm,
total length 98 cm,
working channel inner diameter 1.2 mm,
distal tip outer diameter 2.8 mm,
consisting of:
Intubation Fiberscope 2.8 x 65
Case
Pressure Compensation Cap
Leakage Tester
LIPP Tube Holder
Cleaning Brush
2x Irrigation Adaptor
Suction Valve
Bronchoscope Insertion Tube, size 4, sterile
Bronchoscope Insertion Tube, size 2, sterile
Plug

Retromolar Intubation Endoscope Set, autoclavable, 35,000 pixels,


25
outer diameter 5 mm, for ETT > 5.5 mm, usable
sheath length 40 cm, distal bending 40°, with movable eyepiece,
consisting of:
Retromolar Intubation Endoscope, autoclavable
Tube Holder

Retromolar Intubation Endoscope, with eyepiece, outer diameter 2 mm,


26
for ETT 2.5 - 3.5 mm, usable sheath
length 22 cm,
distal bending 40°,
angle of view 80°,
including tube holder for tube fixation and O2 application
consisting of:
Retromolar Intubation Endoscope 2 x 22
Case
Tube Holder

Plastic Container for Flexible Endoscopes, suitable for gas and


27
hydrogen peroxide (Sterrad®) sterilization and
storage, external dimensions (w x d x h): 550 x 260 x 90 mm, for use with a
flexible endoscope

Airway Trolley, rides on 4 antistatic dual wheels, 2 equipped with


28
locking brakes, for mounting monitors with
VESA 75/100 connection, integrated cable conduit in vertical beam and
cable manager, load capacity for
monitor: max. 18kg Dimensions mobile stand: 670 x 1660 x 670 mm
(w x h x d),
Caster diameter: 100 mm

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consisting of:
Subrack for Mobile Stand
Beam Module, with tube
Drawer
Equipment Rail
Cross Tube Adaptor
Round Pipe, length 25 cm

Holder for Flexible Endoscopes, for mounting to standard tubes,


29
incl. installation accessories

ProShield Protection Tube, for flexible telescopes, for single use,


30
unsterile, distal closed, package of 10, for use
with Holder for Flexible Endoscopes

NOTE:
The system should be FDA/CE/JIS/MHLW approved.
03 years with parts and services comprehensive warranty.
Life span of the quoted model should be clearly defined by the manufacturer.
Technical training as well as operational training must be provided by
the supplier in case if required.
Service manual as well as operational manual must be provided along with
the machine.
PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of the
equipment.

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5.5 TRANS CRANIAL MAGNETIC STIMULATION MACHINE


Clinical
Physiotherapy
Specialty
Generic
Trans Cranial Magnetic Stimulation Machine
Name
Clinical Trans cranial magnetic stimulation (TMS) is a noninvasive procedure that
Purpose uses magnetic fields to stimulate nerve cells in the brain to improve symptoms
of depression. TMS is typically used when other depression treatments haven't
been effective.
TECHNICAL SPECIFICATIONS
 Large color TFT display
 Possibility of manual, automatic, double and repetitive stimulation,
 including burst / theta burst capabilities
 All stimulation data should be shown on the display such as energy,
coil temperature, type of stimulus and trigger
 Types of wave forms: Biphasic and monophasic
 Stimulation frequency up to 50 per second (50 Hz)
 Double stimulation function
 MEP module: 2 channel
 Protocol Management for External PC/Laptop as per manufacturer
recommendation
 Provision for upgradation for Ultrafast stimulation of 100 Hz
Accessories:
 Dedicated chair for comfortable repetitive stimulation sessions
 Butterfly Coil - focal stimulation 70mm
 Cooled Coil - therapy solution for repetitive stimulation sessions,
Butterfly 70mm Air cooled with laminar flow
 Pneumatic stimulation footswitch
 Original Trolley from same manufacturer with Arm Support
Optional:
 Circular Coils for diagnostic solution, Circular 90mm with
Integrated controls and display
 Circular Coils for diagnostic solution, Circular 70mm with
Integrated controls and display
 Butterfly Coils - For focal stimulation, 70mm, Placebo with
Integrated controls and display
 Butterfly Coil with 90° Handle - 70mm with 90° Handle Comfortable
 Double-Cone Coil - for maximum depth Double-Cone 110mm
with Integrated controls and display
 Cooled Coils - therapy solution for repetitive stimulation sessions
Butterfly 70mm, Placebo Air cooled with laminar flow
 Cooled Coils - therapy solution for repetitive stimulation sessions
Circular 70mm Air cooled with laminar flow
 Cooled Coils - therapy solution for repetitive stimulation sessions

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Double-Cone Air cooled with laminar flow


 Stimulation Frequency up to 100Hz
 Robotic chair for maximum patient’s comfort

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the
manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided along
with the machine.
 PPM Schedule should be share with Biomedical Engineering Department
along with the supply of equipment, which will include calibration and
validation of the equipment.

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5.6: BABY RESUSCITATION SYSTEM

 Clinical Specialty Nursery, Paeds


 Generic NameBaby Resuscitation System
 Clinical Purpose The aim of neonatal resuscitation is to prevent neonatal death and
adverse long-term neurodevelopmental sequelae associated withperinatal asphyxia.

 TECHNICAL SPECIFICATIONS
 · Heating module equipped with 2 heating bodies 600watt, halogen areal
illumination and space for a phototherapy installation.
 · Treatment bed with measures: 50x80cm or better with side panels. .
 ● Electronic proporational servo regulator, with temperature probe.
 ● Mobile central stand with electric distributions
 ● Treatment bed with detachable plastic side shields and adjustin to an uphold and
drainage(Trendelenburg) position. Washable mattress.
 ● The heating module is 90◦ revolvable for X-Ray.
 ● Three hight adjustable shelves placed above the treatment bed.
 ● Two drawer under the treatment bed oxygen cylinder holder
 · X-Ray Tray under the treatment bed.
 · Time Module-medical watch with the Apgar signalization
 · Oxygen suction pump with under pressure system with tubing and 1 liter
collection jar with lid.
 · Temperature setting range of 32-37◦C with the accuracy of 0.1◦C.
 · Auto and manual mode
 · LCD/LED Display
 · Display range 20-45◦C
 · Audio and visual alarms
 · IV Pole

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 5.7: PHOTO THERAPY MACHINE

 Clinical Specialty Nursery, Paeds


 Generic NamePhototherapy Machine
 Clinical Purpose Phototherapy Units teat hperbilirubinemia by irradiating the baby
with light in the blue regon of the spectrum from 420-500 nm. This light oxidizes the
billirubin in the blod, thus producing compounds that can be elinated froc the body.

 TECHNICAL SPECIFICATIONS
 Phototherapy unit Controlled by a microprocessor and touch screen LCD display.
 Builtin counter of worked hours informs staff about the upcoming service control of
devices
 Irradiance source: high power LED modules working in two modes, continuous and
intermittent mode.
 Waelength: 450-470nm Irradiance level: more than 50µW/cm2/nm, distance 50cm
 Estimated life: minimum 60000 hours or more
 Operative hight: 40-90cm from bed or more
 Illuminated area: 600x300m or more.
 Timer: from 10minutes to 24 hours or more.
 Temperature monitor skin sensor accuracy +0,1 ◦C or better
 Signal: when the temperature exceeds 38.5◦C or better
 Height setting : mobile stand 125-175cm and tilting.
 Working heights of the device: 45-90cm from the bed surface
 Power consumption: maximum 150W or better.

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5.8 INFANT INCUBATOR


Clinical Specialty Nursery, Paeds
Generic Name Infant Incubator/Baby Incubator
Clinical An incubator is designed to provide a safe, controlled space for infants to live
Purpose while their vital organs develop. Unlike a simple bassinet, an incubator provides
an environment that can be adjusted to provide the ideal temperature as well as
the perfect amount of oxygen, humidity, and light.

TECHNICAL SPECIFICATIONS
 Microprocessor based servo controlled temperature system
 Control modes: Air mode and baby skin mode
 Humidity control system, oxygen concentration display system
 LED Display of Set temperature, Air temperature, baby skin temperature,
humidity, oxygen concentration, timer and heating power.
 Self - testing function, various failure alarms by audible and visual
 >37° temperature set function
 Embedded integrated sensor module
 Triple protection for over temperature with separate cut off device,
more safety system
 The inclination of infant bed is adjustable
 Double wall hood, 4 operating windows and 2 iris ports
 Independent locking device for front door
 RS232 connector, Oxygen inlet

Optional :
 X ray cassette Tray
 Baby Weight System
 Electric height adjustable
 LED phototherapy unit
 Air and oxygen blender
Power Supply AC110/220V 60/50Hz
Power Input 420 VA

Operating Conditions
Environment Temperature 20°C ~ 30°C
Environment Relative humidity 30% ~ 75% RH
Environment Air Velocity of flow < 0.3m/s
Air Temperature Control range 25°C ~ 38°C
Skin Temperature control range 32°C ~ 38.5°C
Humidity display range 0% ~ 100% RH
Humidity Control range 20% ~ 60% RH

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Oxygen Concentration display range 10% ~99%


Skin Temperature sensor accuracy ±12°
Temperature fluctuation ±0.5°C
Uniformity of mattress temperature <0.8°C
Warm-up time < 45min
Internal noise level <55dB (A) or better
Infant bed tilt angle ±10°
Mattress Size 65cm (L) x 37cm (W) or better
Trough capacity 1200ml
Air filter 0.5um or better

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by
the manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided
along with the machine.
 PPM Schedule should be share with Biomedical Engineering
Department along with the supply of equipment, which will
include calibration and validation of the equipment.

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5.9 DIGITAL 3 CHANNEL ECG


Clinical Specialty Cardiology, ICU, Wards
Generic Name ECG Machine (3 Channels)
Clinical Purpose An electrocardiogram (ECG) is one of the simplest and fastest tests
used to evaluate the heart. Electrodes (small, plastic patches that stick to
the skin) are placed a certain spots on the chest, arms, and legs. The
electrodes are connected to an ECG machine by lead wires.
TECHNICAL SPECIFICATIONS
 3.5'' or more TFT screen
 12 leads simultaneous display
 Thermal printing system
 Power supply both AC and DC
 High capacity built-in lithium rechargeable battery
 Battery power supports continually record 150 pieces of ECG
 Built-in Database
 Store more than 800 pieces of archive
 Digital signal processor for filter
 Auto-measurement,auto-analysis and auto interpretation functions
 Lead: Standard 12 leads
 Patient leak current: <10uA
 Input impedance: >=50M
 Frequency response: 0.05Hz-150Hz(-3dB)
 Time constant: Time constant>3.2s
 CMRR: 100dB
 Dimension of recording paper: 80mm(w)x20m(L)paper
 Paper speed: 25mm/s,50mm/s
 Sensitivity choice: 5,10,20mm/mV.Standard sensitivity is 10mm/mV+0.2mm/mV
 Measurement parameters : HR,P-R interval , PDuration, QRS
 Duration,
Q-T interval,Q-Tc,P Axis,QRS Axis,T Axis,R(V5), S› (V1),R(V5)+S(V1)
 Product safety type: Class 1.Type CF, there is defibrillation and
pacing protection circuit.
 Enduring polarization voltage: +300mV
 Noise level: ≤15µVp-p
NOTE: The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided along
with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along
with the supply of equipment, which will include calibration and validation of
the equipment.

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5.10 DIGITAL 12 CHANNEL ECG


Clinical
Specialty
Cardiology, ICU, Wards
Generic
Name
ECG Machine (12 Channels)
Clinical An electrocardiogram (ECG) is one of the simplest and fastest tests used to
Purpose evaluate the heart. Electrodes (small, plastic patches that stick to the skin) are
placed at certain spots on the chest, arms, and legs. The electrodes are connected to
an ECG machine by lead wires.

TECHNICAL SPECIFICATIONS
 Display: 5" or more TFT, touch screen, led backlight
 Lead: Standard 12 leads
 Patient leak current: <10 micro A
 Input Impedance: >50ΜΩ
 Frequency response: 0.05Hz ~ 150Hz (-3dB)
 Dimension of recording paper : 210mm (W) x 20m (L) high-speed
 thermal paper
 Paper speed : Auto record : 25mm/s, 50mm/s, error : ±5%
 Measurement parameters : HR, P-R. interval, P Duration, QRS Duration, T Duration, Q-T
interval, Q-Tc, P Axis, QRS Axis, T Axis, R(VS), S(VI),
R(VS) + S(VI)
 Memory : 1 ECG cable, 1 ground wire, 1 set limb electrode clamp
1 paper roll, 1 set chest electrodes, Power connection USB
connection, Software (same languages as internal software)
Manual: GB, FR, IT
 CMRR : > 60dB, > 100dB (Adding Filter)
 Time constant : Time constant > 3.2s
 Input Way : Floating and defibrillation protection
 CMRR : > 60dB, > 100dB (Adding Filter)
 EMG interference filter : 35 Hz (-3dB)
 Recording way : Thermal printing system
 Rhythm record : 25mm/s, 50mm/s, error : ±5%
 Manual record : 5mm/s, 6.25mm/s, 10mm/s, 12.5mm/s, 50mm/s,
error : ±5%
 Sensitivity selections : 5, 10, 20, 40mm/mV, error : ± 5%.
Standard sensitivity is 10mm/mV ± 2mm/mV.
 Auto record : Record setup according to auto record format and
mode, automatically changing leads, measuring and analyzing.
 Rhythm record : Record setup according to rhythm record format
and mode, automatically measuring and analyzing.
 Manual record : Record setup according to manual record format,
manually changing leads.
 Product safety type : Class I CF applied part; there is defibrillation
and packing protection circuit in it.

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 Enduring polarization voltage : ± 500mV


 Noise level : <15μVp-p
 Power supply / Frequency : AC : 100 – 240V, 50/60Hz DC:14.8V,
3700mAh rechargeable lithium battery

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined
by the manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided along
with the machine.
 PPM Schedule should be share with Biomedical Engineering
Department along with the supply of equipment, which will
include calibration and validation of the equipment.

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5.11 DIGITAL 6 CHANNEL ECG

Clinical Specialty Cardiology, ICU, Wards


Generic Name ECG Machine (6 Channels)
Clinical Purpose An electrocardiogram (ECG) is one of the simplest and fastest tests used to
evaluate the heart. Electrodes (small, plastic patches that stick to the skin)
are placed at certain spots on the chest, arms, and legs. The electrodes
are connected to an ECG machine by lead wires.
TECHNICAL SPECIFICATIONS
 5" or more TFT, touch screen, led backlight
 Digital isolation technology and signal processing solution, digital filter
 Patient management, name and age and id.
 Detail analysis report.
 Multi-language options: German, French, Italian, Turkish
 Built-in lithium rechargeable battery, wide thermal printing system
 USB and LAN socket.
 Memory: Built-in memory or mini SD Memory card. Store more
than 1000 pieces of archive
 Auto-measurement, auto-analysis, and auto interpretation.
 Lead: Standard 12 leads
 Patient leak current : <10 micro A
 Input impedance : ≥50 MΩ
 Frequency response : 0.05 ~ 150HZ(-3dB)
 Time constant : >3.2S
 CMRR : >100dB
 Dimension of recording paper : 80mmx20m
 Paper speed : 25mm/s, 50mm/s
 Sensitivity choice : 5, 10,20mm/mV.
 Measurement parameters : HR, P-R interval, P-Duration, QRS
Duration, Q-T interval, Q-Tc,P Axis, QRS Axis, T Axis, R(V5),
S(V1), R(V5)+S(V1)
 Product safety type : Class I, CF. Defibrillation and pacing protection
 Enduring polarization voltage : ±300mv
 Noise level : <15uVp-p
 Memory: Built-in memory or mini SD Memory card. Store more
than 1000 pieces of archive
 CMRR : >100dB
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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5.12 BABY RESUSCIATION APPARATUS


Clinical
Specialty Nursery, Paeds, Labor room, Gynae
Generic
Baby Resuscitation Trolley/Infant Resuscitation Trolley
Name
Clinical It is specially designed trolley used in nursery including oxygen, warmers and
Purpose other related items for the cure and care neonates and paeds.

TECHNICAL SPECIFICATIONS
 Pre-warming mode, manual mode and baby mode controlled by
micro-computer
 LCD display with temperature data storage and curve display function
 Multiple failure alarm indication
 Horizon angle of heater head and bassinet inclination adjustable
 Built-in LED phototherapy function
 Panels around bassinet can be turned outward
 Silicon mattress can be warmed and temperature is controllable
 APGAR timer
 Vertical Height Adjustment (VHA) stand
 Power Supply: AC220V-230V/50Hz
 Maximum Power Output: ≤900VA or better
 Control Mode: pre-warming mode, manual mode and baby mode are
controlled by micro-computer)
 Baby Mode Temperature Control Range: 34.5-37.5°C or better
 Adjustable Range of Mattress Warming: 25-38°C or better
 Temperature Uniformity of Mattress: ≤2°C or better
 Angle of Warming Module: ±60° or better
 Bassinet Inclination: maximum angle of upward tilt; 20°, maximum
angle of downward tilt; 20°
 Accuracy of Skin Temperature Sensor: ±0.3°C
 APGAR Timer: emits audible tones at 1’, 5; 10’ increments
 Failure Alarms: over temperature alarm, deviation alarm, sensor failure
 alarm, power failure alarm, setting alarm, checking alarm and many more
 Maximum Billirubin of Radiation on Mattress (effective range): 0.8mw/cm2
 Billirubin Uniformity of Radiation on Mattress (effective range): >0.4

Standard Configuration:
 Main Unit (warming module, controller, bassinet, main column and VHA
stand)
 Skin Temperature Sensor
 IV Stand
 Silicon Mattress

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 Trays & Panels


NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined
by the manufacturer.
 Technical training as well as operational training must be provided
 by the supplier in case if required.
 Service manual as well as operational manual must be provided along
with the machine.
 PPM Schedule should be share with Biomedical Engineering
 Department along with the supply of equipment, which will
include calibration and validation of the equipment.

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5.13 PLASMA APHERESIS MACHINE


Clinical
ICU, HDU, Hematology
Specialty
Generic Name Plasma Apheresis Machine
Clinical An apheresis machine is a device which receives blood removed from a
Purpose patient or donor's body and separates it into its various components:
plasma, platelets, white blood cells and red blood cells.

TECHNICAL SPECIFICATIONS
 Latest Blood Component Collection Technology
 Portable Apheresis system for cell therapy.
 Therapeutic Apheresis.
 Transfusion Medicine.
 Programmable Microprocessor Controlled.
 Applicable to both adults and paeds.
 Discontinuous flow centrifuge system.
 Single needle for all type of application protocols.
 Aphaeresis options to collect Platelets, Red Blood Cells, Plasma &
Stem Cells
 Leukodepleted platelets in a fully automated procedure
 Ease of use & flexibility
 Data acquisition capability
 Upgradeable Software & compatible with new generation of kits
 26 kg weight
 Single Access
 Power: 550W
 Centrifuge Speed: 3000-7000 RPM
 Inlet Flow ml/min: 20-100
 Anticoagulant Ratio: 1:8 – 1:16
 Closed & Open Apheresis Kits available
 Monitors & Alerts: 4 air detectors, 2 pressure monitors,
2 spill sensors, 2 separation sensors.
 Self-Regulating Flow
Standard Protocols
 Leukodepleted Platelets & Plasma
 Therapeutic Plasma Exchange

Optional Protocols
Blood Component Collection
 Platelet Poor Plasma
 Fresh Frozen Plasma
 Leukodepleted Platelets & Red Blood Cells

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 Red Blood Cells & Plasma


Therapeutic Collection
 Peripheral Blood Stem Cells
 Bone Marrow Concentrate
Autologous Pre-Operative Collection
 Plasma Erythrocyte Saver (2 Buffy coat depleted RBC units
+ 2 FFP units)
 Autologous Erythro-Apheresis (3 Buffy coat depleted RBC units)

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined
by the manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provided
along with the machine.
 PPM Schedule should be share with Biomedical
Engineering Department along with the supply of equipment,
which will include calibration and validation of the equipment.

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5.14 OPG MACHINE WITH CEPH


Clinical
Dental
Specialty
Generic
OPG Machine with Ceph
Name
Clinical
Purpose OPG (Orthopantomogram) machine is a panoramic scanning dental X-ray of
the upper and lower jaw. Panoramic x-rays allow images of multiple angles to
be taken to make up the composite panoramic image, where the maxilla
(upper jaw) and mandible (lower jaw) are in the viewed area.

TECHNICAL SPECIFICATIONS
 Motorized 3-point head fixation with automatic opening on completion
of exposure
 Integrated temple width measurement ensures automatically a
 patient specific orbit
 Patient immobilization positioning (1x forehead and 2x temple supports)
 Automatic Patient positioning by Occlusal bite block, Chin Support and
02 laser beam system
 Control Mirror for patient positioning
 Tray for jewelry and drawer for accessories
 Automatic adjustment to the jaw width
 Automatic radiation management for different images
 Directly connectable to the network (Should has its own IP)
 Color Touch Screen user interface can be swiveled and tilted
 Remote control with LCD to show exposure parameters and dual
exposure button
 4 Patient sizes
Programs:
 Panoramic Programs:
 For adult:
 Artifact reduced for adult
 Constant magnification 1.25x for adult
 With ascending rami
 Artifact reduced without ascending rami
 Constant magnification 1.25x for adult without ascending rami
For children:
 Artifact reduced for children
 Constant magnification 1.25x for children
 Thick slice for anterior tooth region
 Bitewing in the posterior tooth region
 Bitewing in the anterior tooth region
 Lateral view of TMJ with mouth open and closed
 Lateral view of TMJ ascending rami

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 Paranasal sinuses
 Paranasal sinuses, linear slice orientation
 Quick shot program: PAN 9.1 sec & CEPH 4.7 sec.
Ceph Programs:
 Posterior-anterior, symmetrical
 Anterior-posterior, symmetrical
 Lateral Ceph (size 18x23cm) asymmetrical
 Lateral Ceph full format (size 30x23cm)
 Carpus view, symmetrical
Technical data:
 3D resolution in HD mode: 80 μm or better
 3D Volumes in single shot without stitching:
 Ø5x5.5cm for local findings and endodontic or single implants
 Ø8x8cm for lower and upper jaw dentition for multiple implants
 Ø11x10cm for complete dentition including wisdom teeth
 Ø17x13cm for complete dentition including both Temporomandibular
joints and cranial base.
 Modes: Low Dose, Standard and High Definition
 3D Sensor: Flat panel detector
 2D Sensor: DCS with autofocus function
 Scan time: 2-5 sec. or better
 Exposure time: 14 sec. or better
 Re-construction time: approx. 1.5 min. or better
 Visualization time: approx. 4.5 min. or better
 Patient position: Standing / sitting
 KV range: 60-90 KV
 mA range: 3-16 mA
 Imaging software: DICOM compatible
 Built-in compartment for storage of bite blocks and accessories
 Ambient multi-color light system
Software:
 Manufacturer’s own Image processing software and storage of
patient data including images. This software should be compatible
with Practice Management Software. It should be capable to Import
DICOM, STL as well as export of DICOM data for 3rd Party software
 Built-in metal artifact reduction software
 Implant planning software including implant library, Nerve locator
and Reporting
 Endodontic software
 DICOM printing software to print the images on DICOM Printer
 Application for iPad to see the images connected to central database
 Dedicated Reconstruction PC original from manufacturer

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ACCESSORIES:
 Branded Workstation PC with following configurations:
 Ci7 Latest Generation, 16GB RAM, 2TB Hard Disk, 2GB Dedicated
Graphic Card & 19” FHD LED Monitor with Keyboard & Mouse
 Pure Sine wave Online UPS to take load of X-ray, PC and DICOM
Printer with 10-15 Backup time
 DICOM Printer (Laser Imager with 2x Trays)
 Film Sizes (inch) 8x10, 10x12, 11x14 & 14x17
 (3 Dedicated Sensors: 1x CBCT, 1xPAN & 1xCEPH)

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined
by the manufacturer.
 Technical training as well as operational training must be provided
by the supplier in case if required.
 Service manual as well as operational manual must be provide
 along with the machine.
 PPM Schedule should be share with Biomedical Engineering
Department along with the supply of equipment, which will
include calibration and validation of the equipment.
 PNRA Registration will be responsibility of the supplier

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5.15 HANDS-INSTRUMENTS FOR SPINE SURGERY

Clinical Specialty Operation Theater


Generic Name Hands Instruments for Spinal Surgery System
Clinical Purpose It should provide complete set for Endoscopic Spine Surgery which
should include Transforaminal, Intra-laminar & posterolateral
approach.

TECHNICAL SPECIFICATIONS
Transforaminal Endoscope
 Wide Angle Telescope 25°, angled eyepiece, outer diameter 6.6 mm, working channel 3.6 mm, length
25.7 cm, autoclavable, fiber optic light transmission incorporated.
 Operating Sheath, graduated, with distal beak, integrated irrigation connector, inner diameter 6.8
mm, outer diameter 7.8 mm, length 25 cm, for use with Telescope.

 Operating Sheath, graduated, distal oblique, integrated irrigation connector, inner diameter 6.8 mm,
outer diameter 7.8 mm, length 25 cm, for use with Telescope.
 Puncture Needle, including stylet, Ø 1.8 mm, working length 25 cm, with 1.3 mm opening for guide
wire
 Guide Wire, blunt, Ø1,1mm, working length 45cm
 Dilation Sleeve, outer diameter 6.5 mm, inner diameter 1.4 mm, length 31 cm, with two ports, for the
transforaminal approach.

 Plastic Container for Sterilizing and Storage, perforated, with transparent lid, with inserts for two
angeled rigid telescopes, external dimensions (w x d x h): 515 x 240 x 84 mm.

Interlaminar & Posterolateral Endoscope


 Wide Angle Telescope 25°, angled eyepiece, outer diameter 6.6 mm, working channel Ø 3.6 mm,
length 18 cm, autoclavable, fiber optic light transmission incorporated.

 Operating Sheath, graduated, with distal beak, with clamp mechanism for fixation, integrated
irrigation connector, inner diameter 7.2 mm, outer diameter 7.9 mm, length 18 cm, for use with
Telescope 25°.
 Operating Sheath, graduated, distal oblique, with clamp mechanism for fixation, integrated irrigation
connector, inner diameter 7.2 mm, outer diameter 7.9 mm, length 18 cm, for use with Telescope 25°.
 Puncture Needle, including stylet, Ø 1.8 mm, working length 18 cm, with 1.3 mm opening for guide
wire.
 Guide Wire, blunt, Ø1,1mm, working length 31 cm
 Dilation Sleeve, outer diameter 6.5 mm, inner diameter 1.4 mm, length 22 cm, with two ports, for the
interlaminar approach.
 Plastic Container for Sterilizing and Storage, perforated, with transparent lid, with inserts for two
angeled rigid telescopes, external dimensions (w x d x h): 515 x 240 x 84 mm.
Spine Instruments
 Dissector, Ø 2,6 mm, working length 36 cm, distally 45° bended.
 Dissector, Ø 2,6 mm, working length 36 cm, distally 90° bended.

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 Palpation Hook, distally angled 45°, diameter 2 mm, working length 34 cm.

 Palpation Hook, rotating, dismantling, not insulated, without connector pin for unipolar coagulation,
with irrigation connector for cleaning, with distal ball, bendable to 90°, size 2.7 mm, length 36 cm
consisting of: Metal Handle, without ratchet, with plastic rings with larger contact area outer Sheath
with Working Insert.
 Distal hook, rotatable, single action jaws, size 3.5mm, working length 36cm, consisting of:Plastic
Handle, without ratchet with connector pin for unipolar coagulation, Biopsy forceps insert with distal
hook, working length 36 cm, diameter 3.5 mm.
 Grasping Forceps, rotating, dismantling, insulated, with connector pin for unipolar coagulation, with
LUER-Lock-adaptor for cleaning, single action jaws, fenestrated, size 3 mm, length 36 cm, consisting
of:Plastic Handle, without ratchet outer Sheath, with forceps insert.
 CLICKLINE Palpation Hook, with distal ball, bendable to 90°, with irrigation connector for cleaning,
diameter 3.5 mm, working length 36 cm, consisting of: Metal Handle, without ratchet outer Sheath
with Palpation Hook Working Insert.
 Bipolar Electrode, angled, diameter 2.5 mm, working length 36 cm consisting of: Bipolar Electrode
Insert, Sheath for Bipolar Electrodes Bipolar Spring Handle.
 Bipolar High Frequency Cord, length 300 cm
 Bipolar High Frequency Cord, length 300 cm,
 Take-apart consisting of: Handle, Insert, Spoon Forceps.
 Take-apart Grasping Forceps, diameter 2.3 mm, working length 30 cm, consisting of: 28169 A Handle
28063 SE Insert, Grasping Forceps
 Grasping Forceps, serrated jaws, diameter 2.3 mm, working length 30 cm, consisting of: Handle,
Insert, Grasping Forceps.
 Punch, dismantling, 45° downbiting, not through-cutting, diameter 3.5 mm, working length 30 cm
consisting of:Punch Insert, Outer Sheath, Metal Handle.
 Punch, dismantling, 90° downbiting, not through-cutting, diameter 3.5 mm, working length 30 cm
consisting of:Punch Insert Outer Sheath Metal Handle.
 Grasp. Forceps, with jaws, with 90° angle of view, Ø 3.5 mm, working length 36 cm Fasszange, ein
Maulteil beweglich
 Grasping Forceps, double action jaws, diameter 2.7 mm, working length 36 cm
 Trephine, with round handle, inner diameter 3.2 mm, outer diameter 4.2 mm, working length 22 cm.
 Trephine, with round handle, inner diameter 7 mm, outer diameter 8 mm, working length 17.5 cm.
 Trephine, with pyramidal handle, inner diameter 1.6 mm, outer diameter 2.7 mm, working length 30
cm.
 Bipolar High Frequency Cord, length 300 cm.
 Punch, bendable, single action jaws, diameter 3.5 mm, working length 36 cm.
 Grasping Forceps, bendable, single action jaws, Ø 3.5 mm, working length 36 cm.
 Operating Sheath, distal 45° oblique, integrated irrigation adaptor, outer diameter 7.5 mm, inner
diameter 6.8 mm, length 17 cm, for use with Telescope 25°.
 Metal Mallet, with plastic replacement head, length 22.5 cm.
 Punch Sleeve, for use with operating sheaths.

 Fixation Handle, for adjustment of dilation sleeves with outer diamter 2.5 - 6.5 mm.

 Plastic Container for sterilization & storage of variable instrument sets, perforated, with transparent
lid, silicone mat, two-level storage, (1 additional insert), external dimensions (wxdxh): 545 x 260 x
115 mm consisting of: 2x snap-in clip, package of 12 2x silicone tie-downs, package of 12 Tool The
plastic containers are suitable for steam, gas and hydrogen peroxide sterilization.
Minimal invasive spine set.

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Short Scope
 Forward-Oblique Telescope 25°, eyepiece angled 90°, diameter 4 mm, length 6 cm, autoclavable, fiber
optic light transmission incorporated, for use with 4 cm long.
Trocars for Short scope
 Trocar, diameter 15 mm, working length 40 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 6 cm.
 Trocar, diameter 19 mm, working length 40 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 6 cm.
 Trocar, diameter 23 mm, working length 45 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 6 cm.
Medium Scope
 Forward-Oblique Telescope 25°, eyepiece angled 90°, diameter 4 mm, length 9 cm, autoclavable, fiber
optic light transmission incorporated, for use with 7 cm long.
Trocars for Medium scope
 Trocar, diameter 15 mm, working length 70 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 9 cm.
 Trocar, diameter 19 mm, working length 70 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 9 cm.
 Trocar, diameter 23 mm, working length 75 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 9 cm.
Long Scope
 Forward-Oblique Telescope 25°, eyepiece angled 90°, diameter 4 mm, length 11 cm, autoclavable,
fiber optic light transmission incorporated, for use with 10 cm long.
Trocars for Long scope
 Trocar, diameter 15 mm, working length 90 cm, for use with Trocar Attachment Telescope Holder and
Forward-Oblique Telescope 25°, 4 mm, 11 cm.
 Trocar, diameter 19 mm, working length 90 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 11 cm.
 Trocar, diameter 23 mm, working length 95 mm, for use with Trocar Attachment Telescope Holder
and Forward-Oblique Telescope 25°, 4 mm, 11 cm.
Trocars Attachment
 Trocar Attachment, diameter 15 mm, for use with Trocars.
 Telescope Holder, Ø 15 mm, for use with Trocar Attachment.
 Trocar Attachment, diameter 19 mm, for use with Trocars.
 Telescope Holder, Ø 19 mm, for use with Trocar Attachment.
 Trocar Attachment, diameter 23 mm, for use with Trocars.
 Telescope Holder, Ø 23 mm, for use with Trocar Attachment.
MIS Spine Instruments
 Dilation Sleeve, graduated, inner Ø 1.5 mm, outer diameter 5.2 mm, length 23 cm.
 Dilation Sleeve, graduated, inner Ø 5.3 mm, outer diameter 8.9 mm, length 21 cm.
 Dilation Sleeve, graduated, inner Ø 9 mm, outer diameter 12.7 mm, length 19 cm.
 Dilation Sleeve graduated, outer Ø 14.9 mm, inner diameter 12.9 mm, length 17 cm.
 Dilation Sleeve graduated, outer Ø 16.9 mm, inner diameter 15.1 mm, length 15 cm.
 Dilation Sleeve, graduated, inner Ø 17.1 mm, outer diameter 18.9 mm, length 14 cm.

 Dilation Sleeve graduated, outer Ø 20.9 mm, inner diameter 19 mm, length 13 cm.
 KERRISON Bone Punch, dismantling, 40° upbiting, not through-cutting, 4 mm, working length 24 cm.

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 KERRISON Bone Punch, dismantling, 40° upbiting, not through-cutting, 2 mm, working length 24 cm.

 Spoon Forceps, dismantling, robust, oval, spoon size 3 x 10 mm, single action jaws, WL 20 cm
 Spoon Forceps, dismantling, curved 30°, robust, oval, spoon size 3 x 10 mm, single action jaws,
working length 20 cm
 Hook Scissors, single action jaws, diameter 2.5 mm, working length 25 cm.
 Surgical handle, bayonet-shaped with working length 15 cm for blades.
 Bipolar Coagulation Forceps, insulated, bayonet-shaped, tip 1.2 mm, length 23 cm, for use with
Bipolar High Frequency Cords.
 Bipolar High Frequency Cord, length 300 cm.
 Bipolar High Frequency Cord, length 300 cm.
 Bipolar High Frequency Cord, length 300 cm.
 Palpation Hook, straight, distally 10 mm long and angled 90°, with ball, working length 20 cm.
 Nerve Retractor, angled 30°, distal width 5 mm, working length 17 cm.
 Curette, small, curette size (l x w): 2.7 x 4 mm, bajonet-shaped, distal angled 45°, WL 20 cm.
 FERGUSON Suction Tube, with cut-off hole and stylet, LUER, diameter 4 mm, working length 15 cm

 Suction Tube, with cut-off hole and stylet, LUER, working length 15 cm, 2.5 mm.

 Suction Tube, with distal nerve retractor, with cut-off hole, LUER-Lock connector, diameter 2.7 mm,
working length 15 cm.
 Rotation Socket to clamp on the operating table with one already mounted butterfly nut 28172 HRS,
for use with European and United States standard rails, with lateral clamping element for height and
angle adjustment of the articulated stand.
 Articulated Stand, reinforced version, only, L-shaped, with one mechanical central clamp for all five
joint functions, height 48 cm, operating range 52 cm.
 Palpation Hook, diameter 3.8 mm, distally angled 90°, with ball, blunt, working length 20 cm.

 Dissector, sharp, tip angled 15°, with round handle, size 2 mm, length 25 cm
 KERRISON Bone Punch, dismantling, 90° upbiting, not through-cutting, 4 mm, working length 24 cm.

 KERRISON Bone Punch, dismantling, 90° upbiting, not through-cutting, 2 mm, working length 24 cm.
 KERRISON Punch, dismantling, bayonet-shaped, fixed, upbiting 40° forward, 2 mm, WL 17 cm.
 Bipolar Coagulating Forceps, insulated, bayonet-shaped, tip 0.7 mm, length 23 cm, for use with
bipolar high frequency cord.
 Fiber Optic Light Cable, with straight connector, extremely heat-resistant, with safety lock, increased
light transmission, diameter 3.5 mm, length 230 cm, can be used for ICG applications
 Plastic Container for sterilizing, suitable for steam, gas, and hydrogen peroxide (Sterrad®)
sterilization and storage, perforated, with lid, external dimensions (w x d x h): 321 x 90 x 45 mm for
use with two rigid endoscopes up to max. 20 cm working length
 Plastic Container for sterilization & storage of variable instrument sets, perforated, with transparent
lid, silicone mat, two-level storage, (1 additional insert), external dimensions (wxdxh): 545 x 260 x
115 mm consisting of: 2x snap-in clip, package of 12 2x silicone tie-downs, package of 12 Tool The
plastic containers are suitable for steam, gas and hydrogen peroxide sterilization.
Tray For Complete Set (3 Scopes & 9 Trocars & 3 Attachments)
 Wire Tray, for Cleaning, Sterilization and Storage of instruments, stackable, including hole plate wall.s
and foldaway handles, external dimensions (w x d x h): 480 x 250 x 66 mm
 Lip for Wire mash tray 480 x 250 mm.
 Silicone Grid Insert "Large Diamond Grid", blue, extra wide meshed, external dimensions: (w x d): 470
x 240 mm, for the storage of instruments in standard wire trays, plastic and sterilization containers

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 12 Fixation post including screw and washer to screw in to Wire tray for fixation of instruments, to be
used with silicone tie-downs. External dimensions W: 9 x 38 mm.
 Silicone Tie-Downs for use with posts and Combination Pack with 12 pcs.
 Small parts basket
 Container with Microstop for sterilization and sterile storage, 600 x 300 x 110 mm, consisting
of:Sterilization Container Bottom Sterilization Container Lid 2 x Germ retention Disc (MicroStop)
Internal dimensions: (w x d x h) 548 mm x 267 mm x 88 mm.
Suction/ Irrigation system
 Suction/ Irrigation system, with integrated module, suction and irrigation pump, incl. mains cord,
power supply 100 - 240 VAC, 50/60 Hz.
 Neuro Software, License allows for rinsing in the Neuro surgeries
 Tubing Set, for single use, package of 10
 One-Pedal Footswitch, digital, one-stage

Exo-scope

 Exo-scope, with zoom and focus function, integrated illumination and camera orientation correction,
working distance 20 - 50 cm, fiber optic light transmission incorporated, wipe-disinfect able for use
with Camera System
 Fiber Optic Light Cable, with straight connector, extremely heat-resistant, enhanced light
transmission, diameter 4.8 mm, length 550 cm
 Control device with 3D wheel, 4 programmable Buttons and USB Interface, for intuitive control of
camera systems and connected devices. for use with 3D Exo-Scope

 Articulated Stand, reinforced version, only, L-shaped, with one mechanical central clamp for all five
joint functions, height 48 cm, operating range 52 cm, with lock.

 Rotation Socket to clamp on the operating table with one already mounted butterfly nut, for use with
European and United States standard rails, with lateral clamping element for height and angle
adjustment of the articulated stand
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

5.16 FULL UHD 4K SPINE SURGEY SYSTEM

Clinical Specialty Operation Theater


Generic Name Spine Surgey 4K Camera System
Clinical Purpose It should provide an outstanding and stable visual field down to details,
creating anexcellent visualizing experience for the surgeons with true-to-
color images, enabling easier and finer operations.
S.NO. TECHNICAL SPECIFICATIONS
 Camera control unit CCU with integrated electronic image enhancement filters, USB ports
direct Image & Video archiving via USB stick or external hard drive. Possibility of
integrating other technologies with the system on the same platform via additional link
modules (3D, and Flexible Endoscopes)
 4K Module for connecting 4K camera System.
 4K Camera Head, Ultra HD 4K Resolution, Automatic White Balance, Fixed Zoom f-18mm,
Plasma Sterilizable.
 LED light source 175, Cold Light with integrated, high-performance LED and one light
outlet, power supply 100 - 240 VAC, 50/60 Hz including: - Mains Cord - Connecting Cable
can be controlled by camera head buttons.
 Fiber Optic Light Cable, with safety locking device, extremely heat-resistant, Ø 3.5 mm,
length 230 cm.

 56" or Better 4K Monitor, effective max. screen resolution 3840x2180, image format
16:9, power supply 100 - 240 VAC, 50/60 Hz, wall mounting with VESA 100 and 200
adaptor, consisting of: 1x 24VDC power supply, 1x power cord, 1x cable cover, 2x screws
for cable cover, 4x M6 screws for VESA adaptation, on Stand. (Should be from same
manufacturer).
 Equipment Cart, wide, high, rides on 4 antistatic dual wheels equipped with locking
brakes, mains switch on cover, central beam with integrated electrical sub-distributors
with 12 sockets, grounding plugs, Dimensions in mm (w x h x d): Equipment cart: 830 x
1474 x 730, Shelf: 630 x 25 x 510, Caster diameter: 150 mm consisting of: Base Module,
equipment cart wide Cover, equipment cart wide, Beam Package, equipment cart high 3x
Shelf, wide, Drawer Unit with Lock, wide 2x Equipment Rail, long Camera Holder.
(Imported from same manufacturer)
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

5.17: CTG MACHINE


 Clinical Specialty Gynae, Labouroom
 Generic Name CTG Machine / Fetal Doppler
 Clinical Purpose
 Cardiotocography (CTG) is a technical means of recording (-graphy) the fetal hearbeat
(cardio-) and the uterine contractions (-toco-) during pregnancy, typically in the third trimester. The
machine used to perform the monitoring is called a cardiotocograph, more commonly known as an
lectronic fetal monitor.

 TECHNICAL SPECIFICATIONS
 Capable to external monitoring of foetal heart rate (FHR) and maternal uterine activity (UA).

 Alphanumeric display shows FHR1, FHR2 and UCs and alarms


 Automatically detects transducers when they are plugged in.
 Includes remote switch for event marking.
 Automatic self - test on power up.
 System reports with status and alarms.
 Unit includes a battery allowing for >2 hours continuous operation.
 Fetal heart rate monitoring:
 Fetal heart rate detected by ultrasonic transducer/probe.
 Capable of measuring FHR in the 50-240 beats per minute (bpm) range with 1bpm
resolution and 2bpm accurancy.
 Can monitor twins (i.e. has two transducers).
 Includes high/low audible and visual alarms.
 Includes signal quality / loss indicators and alarms (s).
 Provides audible feedback on signal quality.
 Maternal uterine activity monitoring:
 Uterine contractions measured though apressure sensitive transducer.
 Capable measuring relative uterine contractions (Ucs) in the range of 0-100 units with at
least 1 unit resolution and 1 unit accuracy.
 Includes signal loss due to unplugged transducer.
 Printer/recorder:
 Integrated thermal printer with automatic and manual print out modes.
 Prints FHR1, FHR2, Ucs, marked events and parameters and relevant alarms.
 Print speeds include 1,2 and 3cm/min.
 Compatible with z-folded thernal paper.

 supplied with :
 Instruction for assembly, use and maintenance in English, French and Spanish.
 1xPlastic protectice dustcover.
 1xUC Transducer.
 2xFHR ultrasound transducers.
 1x Remote swithc event marker with cable.

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 3xAdjustable transducer belts for ultrasound (2 FHRs) and toco (UC).


 2xBox of thermal recording paper, total 100 z-folded sheets.
 2xBottle of ultrasound gel, approximately 250ml.

 NOTE:
 · The system should be FDA/CE/JIS/MHLW approved.
 · 03 years with parts and services comprehensive warranty.
 · Life span of the quoted model should be clearly defined by the manufacturer.
 · Technical training as well as operational training must be provided by the supplier in
case if required.
 · Service manual as well as operational manual must be provided along with the
machine.

 · PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

S.NO. 6 OPHTHALMOLOGY EQUIPMENT


6.1 OPHTHALMOSCOPE/RETINOSCOPE SET WITH RECHARGEABLE BATTERY HANDLES &
DUAL PORT DESK CHARGER IN CARRYING CASE.
Clinical
Ophthalmology
Specialty
Generic
Ophthalmoscope / Retinoscope
Name
Clinical Ophthalmoscopy (also called fundoscopy) is a test that lets a doctor see inside the back of the eye,
Purpose which is called the fundus. The doctor can also see other structures in the eye. He or she uses a
magnifying tool called an ophthalmoscope and a light source to see inside the eye while
Retinoscopy is the use of a retinoscope to measure a patient's refractive error. Retinoscopy is an
objective method of refraction in which the patient does not need to tell the practitioner how they
see. If instead they ask the patient questions about how she/he sees, that is called subjective
refraction.
TECHNICAL SPECIFICATIONS
Ophthalmoscope
 Lens range +35 to -30D in one step diopter
 5 aperture setting (Macula, Standard,
 Eccentric fixation,
 Slit aperture and a Red free filter),
 Battery handle with Rheostat
 Spare bulb 4V or as per manufacturer
 Polarizing filter
 4000oK Filter
 with dust cover for Ophthalmoscope mirror
Retinoscope
 Bright and wide visual field with reflection free filters
 Rheostatic brightness control
 Endless 360o rotation enabling quick measurement of astigmatic axis
 control for streak width
 Built-in head rest preventing operator's spectacle from getting scratched
4V illumination
 +2D presbyopic lens or equivalent
 With one spare bulb

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.2 SELECTIVE LASER TRABECULOPLASTY FOR TREATMENT OF GLAUCOMA


Clinical
Ophthalmology
Specialty
Generic Laser
Name
Clinical Selective Laser Trabeculoplasty, or SLT, is a form of laser surgery that is used to lower intraocular
Purpose pressure in glaucoma. It is used when eye drop medications are not lowering the eye pressure
enough or are causing significant side effects. It can also be used as initial treatment in glaucoma.
TECHNICAL SPECIFICATIONS
 Laser source: Q-switched, frequency doubled Nd:YAG
 Wavelength: Green 532 nm
 Energy: 0.2 to 2 mJ or better
 Pulse duration:4 ns or better
 Repetition rate: >1 Hz
 Pulse mode: Single pulse
 Aiming beam: 637 nm or better
 Magnification: According to type of slit lamp
 Cooling: Air cooled
With:
 Latina SLT Gonio Lens for Trabeculoplasty
 Slit Lamp
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.3 OPHTHALMIC DIODE LASER WITH INDIRECT OPHTHALMOSCOPE


DELIVERY SYSTEM FOR ROP CLINIC
Clinical
Ophthalmology
Specialty
Generic Name Ophthalmic Diode Laser
Clinical Compact laser emitting diodes of gallium-aluminium-arsenide are now available for
Purpose incorporation into clinical lasers in ophthalmology. These lasers are cheap and have low
running costs. They are portable and their wavelength of emission (810 nm) may be
advantageous in certain clinical situations.
TECHNICAL SPECIFICATIONS
Subliminal (Micro pulse) Cyclophotocoagulation
Laser for R.O.P Treatment
Specifications:
 Laser Source: Solid state technology
 Wavelength: 810nm
 Power at tissue up to: 3W
 Pulse duration: 0.01 s to continuous
 Aiming beam: 635 – 650nm
 Repeat interval: 0.1 – 0.2 – 0.3 – 0.5 – 0.7 s
 Emission modes: Single, repeat, continuous, painting
 subLiminal Mode (duty cycle form 5% to 35%)
 Cooling: by Peltier effect/by Air.
Consisting of:
 Main Console
 Foot pedal with power adjustment
 Protective Goggles
 Push/pull 810 doctor filter for microscopes
Probes:
 Endoprobes steerable 23G 10/Bx
 Endoprobes steerable 25G 10/Bx
 Cyclophotocoagulation Probe
With:
 Laser Indirect Ophthalmoscope attachment (LIO)
Consisting of:
 Keeler wireless Vantage plus Indirect Ophthalmoscope
in carrying case
 Laser adapter with fiber
 15 D Laser Lens
 20 D Laser Lens
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if
required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply
of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.4 CORNEAL TOPOGRAPHY SYSTEM (SCHEIMPFLUG)

Clinical
Ophthalmology
Specialty
Generic Corneal Topography System
Name
Clinical A corneal topography test is quick and painless. During the test, you will sit in front of a lighted
Purpose bowl that contains a pattern of rings, and rest your head against a bar. A series of data points will
be collected, and a color coded image of your corneal shape will be generated on a computer
screen.
TECHNICAL SPECIFICATIONS
Rotating Scheimpflug Camera for Anterior Segment Tomography
The instrument is a Scheimpflug camera which captures Scheimpflug images during a
rotating scan and calculates a 3D model of the anterior eye segment. Important
parameters such like anterior and posterior corneal curvature, total corneal power,
pachymetry, chamber depth, 360o chamber angle, and lens densitometry are calculated
automatically. The non-contact measuring process takes only 1 – 2 seconds and
captures up to 50 single Scheimpflug images (depending on selected scanning mode).
True elevation points are detected and processed to a 3D model of the anterior eye
segment. Its automatic alignment systems accounts for easy operation and repeatable
results.
Rotating Scheimpflug Camera for anterior segment tomography includes:
 Measuring head on XYZ movable base
 Basic software package
 Patient data management software, network compatible
 Head and chinrest
 Windows based software, network compatible
 Power supply unit input 100 – 240 volt, output 5A 1A, power cord
 USB cable
 Operators manual, user guide and interpretation guideline, 2nd edition
 Dust cover
Basic Software
 Scheimpflug image, Scheimpflug images overview
 General overview, Corneal topography, ant. & post.
 Pachumetry, absolute & relative
 Elevation map, ant. & post, 4 maps refractive
 Virtual eye, Iris image & automatic HWTW
 3D chamber analyzer, Tomography
 Topometric, topography based keratoconus detection
 Compare 2 exams
 Compare 2 exams Scheimpflug images
 Indice report.

Module Belin / Ambrosio Enhanced Ectasia:


This module is based on elevation maps and corneal thickness progression to
support in the detection of Keratoconus / Ectasia, for myopic and hyperopic
eyes, designed for virgin eyes

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Electrically height adjustable table:


220, table plate prepared for compatible PC, with cables and transformer /
interface unit fitted between table top and base, build-in Asus WL-330gE Open
Source WalnAccesspoint, build in USB-HD 500GB for data back-up, 908mm x
518mm, height adjustment from 700 – 880mm

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.5 DIODE LASER 810NM (WITH ENDO LASER ATTACHMENT &


CYCLOPHOTOCOAGULATION PROBES)
Clinical
Ophthalmology
Specialty
Generic
Diode laser
Name
Clinical A diode laser lowers the eye pressure by essentially turning off some of the fluid-producing cells
Purpose of the eye. This “turns the taps down” so that there is less fluid produced in the eye, therefore, less
fluid to drain. The build-up of fluid decreases, and so does the build-up of pressure.
TECHNICAL SPECIFICATIONS
Specifications:
Laser Source: Solid state technology
Wavelength: 810nm or better
Power at tissue up to: 3W or better
Pulse duration: 0.01 s to continuous
Aiming beam: 635 - 650nm
Repeat interval: 0.1 0.2 - 0.3 - 0.5 - 0.7 s
Emission modes: Single, repeat, continuous, painting subliminal
Mode (duty cycle form 5% to 35%)
Cooling: by Peltier effect or better technology
Consisting of:
Main Console:
Foot pedal with power adjustment:
Protective Goggles:
Push/pull 810 doctor filter for microscopes:
Probes:
Endoprobes steerable 23G 10/Bx:
Endoprobes steerable 25G 10/BX:
Cyclophotocoagulation Probe:
With:
Laser Indirect Ophthalmoscope attachment (LIO) Consisting of:
Wireless Vantage plus Indirect Ophthalmoscope in carrying case
Laser adapter with fiber , 15 D Laser Lens, 20 D Laser Lens, 28 D Laser Lens
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.6 OPTICAL BIOMETERY


Optical Biometery

Optical biometry is a highly accurate non-invasive automated method for measuring the
anatomical characteristics of the eye. Accurate measurements are critical for determining the
correct power of an IOL before it is implanted during cataract surgery.
TECHNICAL SPECIFICATIONS
SWEPT Source Biometer for non-contact measurement and visualization of axial length of the eye,
corneal curvature and thickness, anterior chamber, lens, retina, pupil and “white to white” with
an integrated PC for the calculation of intraocular lenses and calculation of intraocular lenses
after corneal refractive surgery. Data export possible to a PC or to office management
systems. DIOCOM Gateway which provides additional networking features to EMR systems
(option) included:
Measurement range:
 Axial length 14 – 38 mm
 Corneal radii5 – 11 mm
 Anterior chamber depth 0.7 – 8 mm
 Lens thickness 1 – 10 mm (phakic eye)
 0.13 – 2.5 mm (pseudophakic eye)
 Central corneal thickness 0.2 – 12 mm
 White to white 8 – 16 mm
Display Scaling:
 Axial length 0.01 mm
 Corneal radii 0.01 mm
 Anterior chamber depth0.01 mm
 Lens thickness 0.01 mm
 Central corneal thickness 1 µm
 White to white 0.1 mm
SD of repeatability:
 Axial length 9 µm
 Corneal radii 0.07 D
 Cylinder >0.75 D axis 4.5o
 Anterior chamber depth 10 µm
 Lens thickness 19 µm
 Central corneal thickness 2 µm
 Central corneal thickness 2 µm
 White to white 90 µm
 IOL Calculation Formulas:
 HaigisSuite (includes Haigis, Haigis-L (for eyes following myopic / hyperopic LASIK / PRK
/ LASEK, Haigis-T (for toric IOL power calculation), Hoffer Q, Holladay 2, SRK/T
Interfaces:
 FORUM eye care data management system
 Computer-assisted cataract surgery system CALLISTO eye (via USB & FORUM)
 Data interface for electronic media` record (EMR) / patient management systems (PMS)
 Data export to USB storage media
 Ethernet port for network connection and network printer with:
 Motorized instrument stand.

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NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.7 CORNEAL CROSS-LINKING SYSTEM (CXL SYSTEM)


Clinical
Ophthalmology
Specialty
Generic
Corneal Cross-Linking System (CXL System)
Name
Clinical Corneal cross linking is a minimally invasive procedure that uses ultraviolet light and eye drops
Purpose in order to strengthen the collagen fibers in the cornea. The procedure is used for patients with
keratoconus, a condition in which the cornea grows thin and weak.
TECHNICAL SPECIFICATIONS
Corneal Cross-Linking System (CXL System) with keratoconus, ectasia after LASIK / PRK, pellucid
marginal degeneration, infectious keratitis, sterile corneal melting, bullous keratopathy.
 Slit Lamp Mount
 Intensities: 3, 9, 15, 18, and 30 mW /cm2 or better
 Irradiation modes: pulsed and continuous light
 Pre-programmed CXL and PACK-CXL protocols
 Thickness-adjusted beam profile
 Comes with
 Base: charging station with an integrated UV meter
 Adapters for a multitude of slit lamps
 C-eye Procedure Kit

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in
case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.8 A/B-SCAN OPHTHALMIC ULTRASOUND SYSTEM WITH 50MHZ PROBE


Clinical
Ophthalmology
Specialty
Generic A/B-Scan Ophthalmic Ultrasound System
Name
Clinical There are two main types of ultrasound used in ophthalmologic practice currently, A-Scan and B-
Purpose scan. In A-scan, or time-amplitude scan, sound waves are generated at 8 MHz and converted into
spikes that correspond with tissue interface zones. In B-scan, or brightness amplitude scan, sound
waves are generated at 10 MHz. where as Ophthalmic ultrasonography uses high-frequency sound
waves, which are transmitted from a probe into the eye. As the sound waves strike intraocular
structures, they are reflected back to the probe and converted into an electric signal.
TECHNICAL SPECIFICATIONS
Ophthalmic Ultrasound Scanner, easy to use, intuitively designed touch screen controls.
Specifically-designed drop-down and pop-up menus hide on-screen graphic controls. WIFI,
Ethernet, USB, and Bluetooth allow you connect to other devices.
A-Scan:
 Ultrasound Probe: Sealed A-probe with 10 MHz focused transducer
 Standard probe for immersion or soft-touch probe for direct contact
 with minimal corneal compression
 Scan Modes: Direct contact or immersion
 Manual or Automatic Capture (Cataract, Dense Cataract, Aphakic,
 and Pseudophakic)
 Measurements: Anterior chamber depth (ACD), lens thickness, vitreous, and axial length
 Averages and standard deviation calculated for up to 10 scans per exam
 Configurable zone tissue velocities
 IOL Formulas: Standard: Binkhorst, Regression-II, Theoretic/T, Holladay, Hoffer-Q,
 Haigis Post-Refractive: Latkany Myopic Regression, Latkany
 Kyperopic, Aramberri Double-K
 Lens Selection Lens calculations in 0.25D increments with built-in 1600+ lens database
B-Scan:
 Ultrasound Probe: Sealed 12 MHz B-probes with focused transducers
 Scan Sampling: 256 ray scan
 Scan Controls: Fully adjustable time-varied gain (TVG), Baseline, Log gain,
 Exponential gain (e-gain)
 Scan Angle: 50° Scan Angle
 Scan Position Indicator: One-click selection of axial or longitudinal scan clock position
with eye model confirmation
 Free-form text for scan position details that automatically annotate onto images and video
clips
 Video Clips: Capture and store 50-frame video clips at up to 20 frames per second (fps)
 Replay in real-time, scalable slow motion, or one frame at a time
 Store up to 6 video clips per eye per exam, easily add or remove video clips from exam
record
 Images: Separately save any number of individual frames from video
 clips as images, complete with annotation.
 Measurement: Unlimited measurements using linear calipers and angle measurement tool
 Database: Full-scale patient database with exam record storage

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

 Reports: Detailed customizable exam reports for printing


 Console: Compact and streamline design
 Display: 10.1” high-resolution multi-touch monitor (1280 x 800 pixel)

50MHZ Probe for Anterior chamber analysis, including structure behind iris up to the Posterior
capsule of the lens linear Probe featuring a linear scanning for completer visualization of the
Anterior chamber in one single scan.
General:
 Image Rendering Outstanding B-Scan and UBM image quality using proprietary Enhanced
Focus Rendering (EFR)Continuous interpolative zoom re-renders at each magnification
level for optimized image quality (up to 4x zoom)
 Annotation Automatic annotation of images and video clips
 Database Full-scale patient database with exam record storage
 Create and save individual user profiles with user-selectable defaults
 Reports Detailed customizable exam reports for printing or exporting
 Hard Drive 128 GB SSD solid-state drive
 Connectivity 802.11n dual-band Wi-Fi and Bluetooth 4.0
 GigE Ethernet LAN and USB 3.0 ports
 One touch export images (.jpg), video clips (.avi), and exam reports (.pdf) for referral,
presentation, or EMR
 Printer Any Windows-compatible printer
 Operating System Microsoft Windows 8
 Console Compact and streamline design with 10.1” high-resolution
 multi-touch monitor (1280 x 800 pixel)
 VESA bracket for articulating arm
 Power 240 VAC, 60 Hz auto-switching medical-grade power supply
 With Compatible Laser Printer

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.9 PHACOEMULSIFICATION SYSTEM


Clinical
Ophthalmology
Specialty
Generic Phacoemulsification System
Name
Clinical Phacoemulsification is a modern cataract surgery method in which the eye's internal lens is
Purpose emulsified with an ultrasonic hand piece and aspirated from the eye. Aspirated fluids are replaced
with irrigation of balanced salt solution to maintain the anterior chamber.
TECHNICAL SPECIFICATIONS
 Hexadisq U/S Phaco Handpiece titanium with 4 or more piezo plates, working frequency
of 28 kHz.
 Control panel with glass cover, transparent illuminating display and silicon keys
 20 Surgeons programming with "Para Prog
 Phaco Modulation choice of Pulse, Burst and CMP
 Femto Aspiration & Cortex Model
 Occlusion mode.
 Peristaltic Pump
 Vacuum 0-600mmHg
 Advance SPEEP Pump mode for efficient and safe working
 Vacuum-Override function
 Easy Phaco technology for 1.6mm up to 2.8mm incisions
 Installed software for CMP (Cool Micro Incision Phaco) & CMP of Phaco and Vitrectomy
 Ready for easy tip CO-MICS (Co-axial Micra incision surgery) for 1.6mm surgery
 Built-In HF Capsulotomy
 Twinac dual pneumatic guillotine cutters for Anterior Vitrectomy - 30 to 2400 cuts per
minute.
 Integrated Compressor for Pneumatically driven cutter
 Upgradable to HFDS ab Interno MIGS Technology 18- System attachable to I/V Pole
 Truly Portable and compact system - Weight 5kg.
 The device is controlled by Direct Access Control Panel

NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.10 INDIRECT OPHTHALMOSCOPE WIRELESS SMALL PUPIL


Clinical
Ophthalmology
Specialty
Generic
Indirect Ophthalmoscope
Name
Clinical The binocular indirect ophthalmoscope, or indirect ophthalmoscope, is an optical instrument
Purpose worn on the examiner's head, and sometimes attached to spectacles, that is used to inspect the
fundus or back of the eye. It produces an stereoscopic image with between 2x and 5x
magnification.
TECHNICAL SPECIFICATIONS
New LED light source reproduces clean illumination in Halogen bulb color and eliminates
the filament shadow.
LED light source provides steady illumination for 50,000 hours, free from exchanging the
light bulb.
Light weight palm-size by Nickel Hydroid battery.
The combination of the LED and the tough re-chargeable battery allows 5 times longer
operation with energy saving.
Specifications
 Light source: 3W white LED
 Filter: UV, red-free and cobalt blue
 Illumination area: 3 steps change of 19, 50, 80 mm (at 500 mm front of instrument)
 Illumination: 600 Lx / Max, 300 Lx / Middle (at 500 mm front of instrument with UV
filter)
 Consecutive light time: Approx 5 hours / max about 10 hours / middle
 Rechargeable battery: Nickel Metal Hydride
 Charging time: Approx. 2.5 hours
 Battery life: Approx. 1500 cycles
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.11 ANTERIOR / POSTERIOR VITRECTOMY SYSTEM WITH ENDO LASER

Clinical
Ophthalmology
Specialty
Generic
Vitrectomy System
Name
Clinical During vitrectomy procedures, a surgeon removes some or all of the vitreous humor within a
Purpose patient's eye.The endolaser is most commonly used to create a laser barricade around retinal
tears, surround retinectomy edges or giant retinal tear margins, and deliver scatter panretinal
photocoagulation. For retinal tears, the goal is to achieve 360º of laser encircling the tear.
TECHNICAL SPECIFICATIONS
Fluidic System with three pump modes (Peristaltic Pump, Venturi Pump and SPEEP mode).
Gravity and Active GFI infusion.
Tubing system with integrated closed pressure sensor,
Auto Venting and limitable back flow functions.
Dualinear wireless multifunctional pedal also controlling the integrated laser and specific
assignment.
Easy phaco", CO-MICS and MICS technology with CMP, Pulse, Burst and Linear functions.
Hexadisq Phaco hand piece with 6-piezo plates. functions. 23G, 25G) with linear or progressive
Pneumatically driven Continuous Flow Cutter (20G, 10 to 10000 cut per minute.
Endo Illumination with two independent Goodlight LED and goodlight LED plus source with
adjustable colors' filter free exit and antiglare panoramic lighting. activation with alarm function
and constant Fluid/air changeover via panel or pedal pressure control with compensation
reservoir.
Visco Injection/Extraction by linear pedal control.
RF-Capsulotomy for difficult cases. (Special feature marks)
HFDS (High frequency Deep Sclerotomy) Option for ab interno MIGS (Micro Incision

Glaucoma Surgery) Built in integrated green endo laser 532 nm controlled without extra pedal.
Endo phaco.
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case
if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the
supply of equipment, which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.12: OPERATING MICROSCOPE WITH VIDEO ATTACHMENT BIOM WITH CO-OBSERVATION FOR
POSTERIOR SEGMENT SURGERIES
Clinical Specialty Ophthalmology
Generic Name Operating Microscope
Clinical Purpose An operating surgical microscope is the most important optical instrument in the modern era of ophthalmic
surgeries. It provides the surgeon with a magnified and illuminated high-quality image of the small
ophthalmic structures.
TECHNICAL SPECIFICATIONS
Microscope head / Optical carrier with:
 Linear motorized zoom ratio 1:6
 Motorized fine focusing
 Stereo coaxial SCI fiber optic illumination system or equivalent
 Retinal protection device
 Fully apochromatically corrected optics with high light transmission
 Microprocessor controlled Depth of Focus management system “Deep View” or equivalent
 Fine tilt adjustment of the microscope body
 Motorized XY coupling with auto re-centering
 Objective f=200mm
 Inclinable binocular tube with integrated inverter or as per manufacturer
 Wide field eyepieces 10X with dioptric adjustment
 Dust cover
 Asepsis set
Mobile Floor Stand with:
 Manual coarse focusing through counterbalanced suspension arm
 Source for fiber or without fiber optic halogen illumination 12V 100W or as per manufacturer with
integrated stand-by lamp
 with integrated stand-by lamp
 Adjustable speed of focus, zoom and XY movement
 Multi-function foot control panel, wired
 Binocular stereoscopic assistant’s attachment with joints for
 Binocular stereoscopic assistant’s attachment with joints for inclination, image erection, inclinable
binocular tube with integrated inverter and wide field 10X eyepieces with dioptric adjustment or as per
manufacturer was added in the specifications
 1-Chip HD Video Camera
 Beam Splitter
Non-Contact Retinal Viewing System consisting of
 BIOM 5 / Resight 700 or Equivalent
 Adapter for above Microscope
 Reduction lens f-200
 90 D lens
 Wifi HD lens
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of equipment, which will include
calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.13 PATTERN LASER WITH SLIT LAMP DELIVERY SYSTEM AND VIDEO
ATTACHMENT
Clinical
Ophthalmology
Specialty
Generic Name Pattern Laser with Slip Lamp
Clinical Purpose Pattern Scan Laser refers to a laser delivery system where multiple laser spots of short
pulse duration are delivered in a preset pattern. These pattern scan laser systems were
developed to decrease the treatment times for diabetic retinopathy, especially pan-retinal
photocoagulation.
TECHNICAL SPECIFICATIONS
Laser Source: Solid-state laser diode and cavity
Wavelength: Yellow configuration: 561nm
Power at the Cornea: Yellow: 50 -1500mW,
Exposure Time: Pattern: 10, 20, 30, Single Spot: 0.01 to 8.0 seconds
Patterns:
Linear (2 to 7 spots) or better
Rectangle (2x3, 2x4, 2x5, 2x6, 2x7)
Square (2x2, 3x3, 4x4, 5x5, 6x6)
Triangle (3, 6, 10, 15, 21 and 28 spots)
Circle – filled (7, 12, 19, 27 and 37 spots)
Circle – empty (12, 18, 24 and 30 spots)
Single Half Circle (4, 7 and 10 spots)
Double Half Circle (11, 17 and 23 spots)
Circle Sector 60 (3 to 7 spots)
Circle Sector 120 (5, 7, 9 and 11 spots)
Double Circle Sector 60 (5, 7, 9 and 11 spots)
Double Circle Sector 120 (8, 12, 16 and 20 spots)
Variable curve, double curve and filled sector
Spot Size Pattern: 100 to 500 µm, continuously variable
Single Spot: 50 to 1000 µm, continuously variable
Spot Spacing Pattern: 0 (touching),
0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0 spot-width
Pulse Duration: Pattern: 10, 20, 30 ms
Single Spot: 10 – 8000 ms
Repeat Model: Pattern: N/A, Single Spot: 50 – 1000 ms
Aiming Beam: Red 635nm, adjustable intensity
Magnification: 6x, 10x, 16x, 25x, 40x
Cooling: Air Cooled
With: Original Slit Lamp stand with column and table
Beam splitte
Video adapter with camera
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of equipment,
which will include calibration and validation of the equipment.

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DETAILS SPECIFCATIONS (TENDER OPENING ON 13-04-2022) FY VALID TILL 30-06-2023.

6.14 AUTO KERATO-REFRACTOMETER


Auto refractors are used to measure the degree of refractive error in the eye, and are suited well toward
applications such as differentiating corneal from lenticular aberrations, and assessing pre-and-post refractive
surgery patients.
TECHNICAL SPECIFICATIONS
Auto Kerato-Refractometer with features including: Rotary Prism Technology or equivalent for Unparalleled
Accuracy, Simple to use, 6 or more – inch color LCD Touch screen Panel, Connectable LAN, Smooth Movements,
One Touch Lock, System Chart, Image function, Easy Load Printer, Near Vision Function, Auto focus / Auto-shoot
function, Spherical Equivalent, Compact and Modern design, Variable fixation light control, Measurement for
Cornea / Iris / Pupil Diameter.
Refractive Power Measurement:
Spherical refractive power : -25D to +22D (0.12D / 0.25D steps)
Cylinder refractive power : 0D to ±10D (0.12D / 0.25D steps)
Astigmatic axial angel : 0° to 180 (in 1° or 5° steps)
Minimal measurable pupil diameter : Ø 2 mm
Corneal Curvature Measurement:
Corneal Curvature radius : 5.00 to 10.00 mm (0.01mm step)
Corneal refractive power : 67.50D to 33.75D (0.12D / 0.25D steps)
(Where, corneal refractive power = 1.3375)
Corneal astigmatic refractive power : OD to ± 10D (0.12D / 0.25D steps)
Corneal astigmatic axial angle : 0° to 180° (1° / 5° steps)
PD measurement range : 20 mm – 85 mm (0.5mm step)
Data Transport Terminal : USB (import) / RS-232C (Export) / LAN (Export)
With Pak made electric stand and table top.
Accessories: Printer rolls (02), Chinrest paper (100), model eye, fuses, dust cover (01) and instruction manual.
NOTE:
 The system should be FDA/CE/JIS/MHLW approved.
 03 years with parts and services comprehensive warranty.
 Life span of the quoted model should be clearly defined by the manufacturer.
 Technical training as well as operational training must be provided by the supplier in case if required.
 Service manual as well as operational manual must be provided along with the machine.
 PPM Schedule should be share with Biomedical Engineering Department along with the supply of
equipment, which will include calibration and validation of the equipment.

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