Annexure 1

Technical Specification of ABG Machine – 1 Unit

Sl. Specification of ABG Machine Specification
No. Yes / No
I The Analyzer should have the following electrodes and able to Measure the
following parameters accurately
1 Blood gas parameters pH, pO2, pCO2, Sp02%(measured)
2 Electrolytes parameters
Na+, K+, Cl, Ca++ including ionized Ca++, magnesium
3 Metabolites parameters
a) Glucose, Saturation Oxygen (SaO2), Hemoglobin and Hematocrit
b) Lactate
c) Urea & Createnine
d) Facility for Regular Quality Assessment of the Analyzer
II. Analyzer should have software program to provide following calculated
parameters
a) Bicarbonate (HCO3)
b) Standard HCO3 (standard HCO3)
c) Base Excess of Blood (BE)
d) Base Excess of Extra cellular fluid (BE-Ecf)
e) Oxygen Content (O2Ct)
f) Oxygen Saturation (SO2%)
g) Total carbon dioxide (TCO2)
h) Alveolar to Arterial oxygen tension gradient (AaDO2)
i) Arterial Alveolar oxygen tension Ratio (a/A)
j) Oxygen carrying capacity (O2 Cap)
k) PO2/FIO2 Ratio
l) P50
m) Respiratory index / Quotient
n) Anion Gap (AG)
o) Plasma Osmolality
p) pH/pCO2/pO2 Corrected to patient temperature
III. Sample handling and Reagent
4 The sample volume for measuring all parameters should less than 250
microliter.
5 Analyzer should accept heparinized whole blood, serum or plasma, arterial,
mixed venous and capillary sample for analysis.
6 Analyzer should use liquid calibration method for calibration of all measure
parameters without use of any gas cylinders or humidifiers.
7 Analyzer should have a standby mode (economy mode) with auto wake up
facility to optimize the reagent utilization.
8 Analyzer display should show the reagent indicator to easy identification of
status of reagent.
9 No fixed tests cartridge/cassettes/modules/sensors or package solutions.
10 Analyzer should allow hands free sample introduction with aspiration mode to
analyze.
11 Analyzer should have the possibility for optional remote support.
IV Software and External features
12 Analyzer should have minimum of 5 programmable options for sample
measurement mode with different parameters configuration for selection of
parameters to test as per physician requirement.
13 Analyzer should perform automated ampoule quality control.
14 Analyzer should have LCD monitor display with touch function.
15 Analyzer should have external keyboard, mouse, barcode reader and high end
color printer compatible with software.
16 Analyzer should have minimum inbuilt memory of at least 100 measurements
of ABG tested and also have a USB port/HIS compatibility that enable to
transfer to external computer.
17 Analyzer should display the English language for all values and instruction.
18 All results should be microprocessor controlled and of latest version of
technology.
19 Analyzer should provide flow chart/graph for assisting clinical interpretation
for resident learning.
20 Analyzer should be user friendly and inbuilt onboard training tools including
onboard help system via multimedia video tutorials.
V. Waste bag
21 The Waste container should be sealed to prevent operator biohazard.
VI Consumables
Consumables for all parameters for 500 cases to be proved as Starter pack
functioning over 6 months from the period of installation.
2. Environmental factors
2.1 The unit shall be capable of being stored continuously in ambient temperature
of 0 -50deg C and relative humidity of 15-90%.
2.2 The unit shall be capable of operating continuously in ambient temperature of
10 -40 deg C and relative humidity of 15-90%
2.3 Shall meet IEC-60601-1-2: 2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility orshould comply with 89/366/EEC;
EMC-directive.
3 Power Supply
3.1 Power input to be 220-240VAC, 50Hz fitted with Indian plug
3.2 Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications.(
Input 160-260 V and output 220-240 Vand 50 Hz).
3.3 Analyzer should have the 1 KV UPS systems for blood gas analyzer for a
minimum one hour back up.
4 Standards, Safety and Training
4.1 Must be FDA, CE,UL or BIS approved product, Etc.
4.2 Shall meet the safety requirements as per IEC 60601-2-27:1994—Medical
electrical equipment.
4.3 Manufacturer/Supplier should have ISO certification for quality standards.
4.4 Should have local service facility .The service provider should have the
necessary equipments recommended by the manufacturer to carry out
preventive maintenance test as per guidelines provided in the
service/maintenance manual.
4.5 Back to back warranty to be taken by the supplier from the principal to supply
 spares for a minimum period 10 years.
5 Documentation
5.1 User Manual in English
5.2 Service manual in English
5.3 Log book with instructions for daily, weekly, monthly and quarterly
maintenance checklist. The job description of thehospital technician and
company service engineer should be clearly spelt out.
6 Warranty
6.1 The Equipment including monitor and all accessories including bought out
items should be under WARRANTY for a period of THREE YEARS after
successful commissioning.
6.2 Comprehensive maintenance contract rates for 7 YEARS after warranty must
be quoted for all accessories including bought out items (UPS etc). Terms and
conditions of CMC should be clearly provided. These would be taken into
consideration while comparing price bids
6.3 All essential spare parts should be made available with the local service centre
during the WARRANTY period and all steps should be taken for immediate
servicing to prevent down time.
6.4 A copy of service manual should be available with the local service centre.
7 Installation, commissioning, testing, maintenance and after sales service.
7.1 The equipment and all accessories should be transported, installed, tested and
commissioned at the Department of Obst. &Gynae, WCH Block, Jawaharlal
Institute of Postgraduate Medical Education and Research, Pondicherry
605006 free of cost.
7.2 All spare parts and consumables should be available with supplier or principals
for a period of at least 10 years.
7.3 In case of any change of dealership in future the principals should undertake
the responsibility of maintaining the equipment through the next dealer.
8 Other tender conditions
8.1 Companies to indicate separately and clearly in their technical bids whether
their products conforms / does not conform to each parameter in the
specification and also to the extent it deviates from the specifications.
Compliance Report to be submitted in a tabulated and point wise manner
clearly mentioning the page/Para number oforiginal catalogue/data sheet. Any
technical specification claimed to be present by the company, if not
substantiated with authenticated catalogue/manual, will not beconsidered.
Hence authenticated copies of such catalogue / manual must be included along
with the bid.
8.2 Supplier must provide the list of equipments available for providing calibration
and routine maintenance support as per manufacturer documentation in service
/ technical manual.
8.3 All Essential Spare parts / Consumables rates to be given separately which
may be freezed for next 10 Years.
8.4 Supplier must provide the list of important spare parts and accessories with
their part number and costing.
8.5 Suppliers should have been in the market for at least 3 years and should have a
satisfied user base for this equipment.
8.6 Suppliers must have made a large number of installations in the country in
reputed institutions and preferably in Government Hospitals with a proven
track record of excellent after sales support for this system.
8.7 List of users must be enclosed.
8.8 The supplier must bring the equipment at own expenditure for
demonstration on a given date, failing which tender will be liable to be
rejected.
Note : Quantity Subject to Change.
 Annexure 2

The local supplier at the time of tender, bidding or solicitation shall be required to provide
self-certification (in the format given below), that the item offered meets the minimum local
content and shall give details of the location(s) at which the local value addition is made.

JIPMER Tender Ref. No. OBGY/ABG/2018-19 Date:

“Certified that the following items quoted has more than 50% of value addition in India at
the location(s) mentioned against each and is eligible for purchase preference as per the Govt. of
India “Public Procurement preference to Make in India” order Dt.15.06.2017.

Details of the location(s) at which the

Sl. No Name of the items
local value addition was made.

Authorised Signature:
Name:
Designation: