ITEM SPECIFICATION

ITEM No. : DESCRIPTION :

Delta Monitor for Operating Room

Specification:
1 TECHNICAL SPECIFICATIONS OF O.R MONTIOR, 6 CHANNELS
1-1 All equipment shall be capable of measuring and displaying
waveforms
for the following hospital desired monitored parameters:
1-1-1 ECG
1-1-1-1 NMT (Neuro Muscular Transmission)
1-1-1-2 Respiratory rate
1-1-1-3 Blood pressure (systolic, diastolic, and mean)
1-1-1-4 Body temperature
1-1-1-5 Arterial hemoglobin oxygen saturation (SpO2)
1-1-1-6 Cardiac output
1-1-1-7 Airway gas concentrations
1-1-1-8 Arrhythmia
1-1-1-9 Screen size not less than 10.4” TFT screen
1-1-2 Alphanumeric data shall be displayed for each parameter.
1-1-3 All patient inputs shall be defibrillator protected.
1-1-4 All patient inputs to comply with IEC and UL standards.
1-1-5 All equipment shall be capable of operating under normal
ambient
environmental conditions of 0 to 15oC, 10% to 95% relative
humidity.
1-2 The display section shall be capable of the digital display of
alarm limits for each parameter and the alarm status for each parameter
1-2-1 Control panel shall incorporate programmed softkeys for
control of monitor functions and display modes, remote record
initiation control for all waveforms, controls for waveform, visual and
audible alarms, and standard Alarm/acknowledge/reset controls.
Alarms are to be configured by the hospital as either latching or
nonlatching.
Pressure channels are to have selectable display of individual or
common
scale.
1-3 Monitors must be modular for at least the advanced parameters
other than the basic functions (i.e. other than ECG, NIBP, SPO2, &
Temp).
1-4 Each monitor shall be supplied with a monitor bracket and
necessary
hardware for mounting and a patient cable and lead set.
1-5 Trending of all parameters shall be for up to 24 hours with
Graphic and tabular displays of derived numeric variables shall be
for selectable sample intervals of one minute up to one hour.
1-6 All bedside monitors need to be interfaced with the hospital's
existing information system. Access to individual bedsides can be
obtained through the monitoring system LAN. If this is not
feasible,
 then direct connections to each bedside will be required. Specify
the
best methodology for your system.
1-7 The following modules should be used in configuring an
appropriate
acute care physiologic monitoring system:
1-7-1 ECG
1-7-1-1 All equipment shall comply with the following criteria or
requirements: isolated input ECG/respiration module(s) with 12-
lead
selection, 1 mV calibration, monitor/diagnostic selection, QRS
beeper
with adjustable volume control, digital heart rate display,
adjustable
heart rate alarm, lead-fault alarm, and trace size/position
controls.
1-7-1-2 Monitor(s) shall be able to display multiple leads of ECG
simultaneously.
1-7-1-3 Module(s) must come complete with patient safety cables and
patient-lead set (5&3 leads).
1-7-1-4 Equipment should include an apnea alarm, which is triggered
if no
breaths are detected over a predetermined period of time.
1-7-2 Arrhythmia
1-7-2-1 The arrhythmia monitoring system shall be a computer-based
system
(using either a centralizer on the network or built into each
bedside
monitor or bedside module for the detection and classification of
arrhythmias and paced beats).
1-7-2-2 Each unit shall provided trending, graphic display
editing, and tabular display of arrhythmia parameters.

1-7-2-3 Each unit shall be capable of displaying the following

information without loss on the central station or bedside display
of any
continuous patient waveforms:
1-7-2-4 Display of each patient's alarm and rhythm status, heart
rate,
and alarm limits for arrhythmia-related criteria (e.g., ventricular
tachycardia, PVC runs).
1-7-2-6 Tabular trend display of arrhythmia data for each patient.
1-7-2-7 Unit status display.
1-7-2-8 Each unit shall be fully integrated with both bedside
monitors
and the central station system; that is, all alarms generated by
the
arrhythmia monitoring system shall be displayed on the bedside
monitor
for the patient, as well as the central station.
1-7-2-9 Capability for S-T segment analysis, including trending and
curser control, for user-selectable point of analysis determination
should be included.
1-7-3 Pulse Oximeter
1-7-3-1 Pulse oximetry module(s) shall include capabilities for
measurement of oxygen saturation with percent digital display,
automatic
calibration, low O2 saturation and low signal alarms, and
adjustable
heart rate and saturation alarms with visual display, and probe.
1-7-4 Invasive Blood Pressure (IBP)
1-7-4-1 IBP module(s) shall be suitable for arterial, venous,
pulmonary
artery, wedge, intracranial, and cerebrospinal fluid pressures with
pressure range selection, auto-zero calibration, dual-digital
display for
systolic/diastolic and/or mean pressures, pressure alarm, and
trace
size/position controls.
1-7-5 Noninvasive Blood Pressure (NIBP)
1-7-5-1 NIBP module(s) shall have adult and pediatric blood
pressure
capabilities. At a minimum, they should be able to measure
systolic
pressures up to 250 mm Hg.
1-7-5-2 Module(s) must come complete with one set of adult, large,
thigh,
and pediatric cuffs.
1-7-6 Respiration
1-7-6-1 All equipment shall have the capability to measure
respiratory
rate through at least one of the following methods:
1-7-6-2 Impedance pneumography, which passes a low-current,
high-frequency carrier signal between two ECG electrodes on either
side
of the chest wall.
1-7-6-3 Pressure-sensitive capsule, which is placed on the abdomen
to
detect body surface movements caused by breathing.
1-7-6-4 Thermistor, which is placed near the mouth or nose to
detect the
temperature changes between inhaled and exhaled air.
1-7-6-5 An apnea alarm, which is triggered if no breaths are
detected
over a predetermined period of time, should be included.
1-7-7 End-tidal CO2
1-7-7-1 End-tidal CO2 module(s) shall have capabilities for
measurement
of expired gas concentrations of CO2 with digital percent CO2 and
respiratory rate display, calibration controls, adjustable alarms,
trace
size/position controls, and probe.
1-7-8 Temperature
1-7-8-1 Temperature module(s) shall include digital temperature
display for 0E to 50EC with the ability to use standard YSI 400 or 700
probes.
1-7-8-2 Thermistor probe (a semiconductor whose resistance changes
with
temperature) shall be included.
1-7-9 Cardiac Output
1-7-9-1 Cardiac output module(s) utilizing the thermodilution
principle
shall include digital display of injectate and blood temperatures
and CO consumption constant with injectate volume/temperature controls,
trace size/position controls, and hemodynamic calculations (stroke
volume,systemic vascular resistance, left ventricular stroke work
index).

1-8 Alarms
1-8-1 The physiologic monitoring system should have visual or
audible
alarms to warn operators of any system fault that may cause unsafe
or
erroneous results.
1-8-2 Audible and/or visual indicators should activate when the
display
reading reaches and remains at the alarm limit.
1-8-3 All alarms should be fully explained in the operator's
manual.
1-9 Audible Alarms
1-9-1 Audible alarms should be distinct and easily identified.
1-9-2 Audible alarms should be enabled when the physiologic
monitoring
system is turned on (i.e., the default volume should not be set to
OFF)
and should be clearly audible at any volume setting.
1-9-3 If the alarm volume is adjustable, it should not be possible
to
turn the volume down so low that it is not likely to be heard.
1-9-4 Although an audible-alarm silence is acceptable, the alarm
must
recur automatically if the condition is not corrected.
1-9-5 If an alarm is silenced, a visual display should clearly
indicate
which alarm is disabled.
1-10 Visual Alarms
1-11 Soft keys & Rotary knob control, and not touch screen or any
external control device
1-12 Rechargeable battery for at least 3 hours operating time
1-13 Docking station for secured attachment over the anaesthesia
machine, also for easily unlocking the monitor from the shelf then pick
& go with the patient to the recovery.
1-14 not too heavy for transportation purposes (Max. 6 KG)
End of specification