4th Batch Equipmentv

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT
For KPJ Pahang Specialist Hospital and KPJ Perlis Specialist Hospital
EQUIPMENT 1
Acoustic
Performance
AUDIOMETER, TESTING BOOTH
* As per recommendation by Act

Frequency (Hz)
Noise Reduction in dB
Standard Room
Dimension
External Dimension
Internal Dimension
Door Perimeter
Wall Panel
Thickness
External
Acoustic Infill
Internal
EQUIPMENT 2
SPECIAL
TESTS/TEST
Floor Construction
BATTERY
Thickness
Upper Surface
Bottom Surface
Door Construction
Jack Panel
Standard Features
Environment
1200 W x 950 L x 2100 mmH

1000 W x 750 L x 1800 mmH
710 W x 1780 mmH
100 mm
2.3mm M.S painted with epoxy finishing
60 - 80kg/m3
0.7mm M.S Cold Rold painted with epoxy density
AUDIOMETER,
CLINICAL
Rockwool.
Minimum 2 channel speech, 2 channels Master
Hearing Aid and Auto threshold feature.
100 mm
Auto threshold tests:
3.0
mm M.S c/w structurally reinforced
Available time for patient to respond: Same as tone
Loaded
with vibration isolator acting as Floating
presentation
Floor.
Increment of hearing level: Minimum 5dB.
Flushthreshold
Mountedtest
c/w(Bksy):
magnetic-seal
Auto
3 ringoftip
with sleeve
stereo plug completely
Mode
operation:
Bksy
Rate of level change: Minimum 2.5 dB/s 20%
wired
Smallest increment of level: 0.5 dB
Double glazed observation window

Carpeted floor
Absorptive acoustic ceiling
Lighting & Electrical Connection
Ventilation Silencers for Inlet and Outlet
Jacked panel
Meet IEC-606001-1-2:2001(Or Equivalent BIS)
General Requirements of Safety for
Electromagnetic Compatibility. Or should comply
with 89/366/EEC;EMC directive

EQUIPMENT 3
-
SPECIFICATION
Defibrillation Type
Should have Manual, Synchronized, or AED function.
Should Built in AED (Automated External Defibrillation) with voice prompt.
Built in paediatric paddles under adult paddles for both adult and paediatric
use.
Energy selectable from 2 to 270J.
Charging time to 270J less than 5 seconds
Charge and discharge buttons on paddles as well as front panel
3 LEDs contact indicator when paddles applied is available.
1-2-3 Step instruction on equipment is available.
Discharge test is available.
Output waveform Biphasic Truncated Exponential.
Protection against Sudden Capacitor Failure.
ECG Monitor
Should come with 3 lead ECG monitoring.
Should have Display screen size at least 6.5 inch.
Up to 4 waveforms can be displayed in TFT colour LCD screen.
ECG picked up via paddles or separate ECG leads.
The monitor shall display of the following: Numerical display of heart rate from 20 to 300bpm
DEFIBRILLATOR, BIPHASIC
Lead selection
ECG gain
Synchronization mode
Battery indicator
Available and delivered energy

Non-invasive Pacing
Pacing mode: fixed or demand
Waveform: modified trapezoid
Pulse rate 30 to 180 ppm, 10 ppm step
Pacing current: 0, 8 to 200 mA in 1 mA
Recorder
Should have two channel thermal recorder
Should have Automatic recording at defibrillation or manual recording
Report shall be providing annotation consists of: Date and time
Delivered energy
Power Source
- Rechargeable battery power source as as well as being mains powered 240V/50Hz
- NiMH type battery
Environment
- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety

for Electromagnetic Compatibility. Or should comply with 89/366/EEC;EMC
directive

EQUIPMENT 4
DEFIBRILLATOR, AED
SPECIFICATION
1- FEATURES
- Should have 3 steps to save a life
iTurn on the AED
iiAttach the electrode pads
iiiPress the shock button
- Daily and monthly self-test function is available from main unit, battery and
pads.
- Waveform: Truncated exponential constant power biphasic.
- Output energy range: 50, 70, 100, 150, 200J (at 50ohm).
- Output energy sequence:
i) 150J-200J-200J for adult mode.
ii) 50J-70J-70J for child mode.
- Analyse-to-SHOCK cycle time: less than 8 seconds (when using new battery).
- End of CPR to SHOCK cycle time: less than 8 seconds (when using new battery).
- Automatic internal discharge: the charged energy is discharged in the following
conditions;
- 30 seconds passes after the SHOCK BUTTON starts blinking
- When A pad is disconnected from the AED or patient, System must be turned of
- Normal ECG appears during the self-test
- Battery removed
2- ARRHYTHMIA ANALYSIS
- Should have an accuracy of:
i) 90% or more for VF (sensitivity)
ii) 75% or more for VT (sensitivity)
iii) 95% or more for non-shockable waveform (specificity)
3- BATTERY REMAINING LAMP
- 100%: 4 green lamps light
- 25%: 1 green lamp lights
- 0%: red lamp lights
4- Environment
- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety for
Electromagnetic Compatibility. Or should comply with 89/366/EEC;EMC directive

EQUIPMENT 5
ECG MACHINE, 12 CHANNEL
SPECIFICATION
1- DESIGN FEATURE
- Should have 12-channel recording
- Should have LCD display in Colour
- Should have data transfer to PC by SD memory or LAN Connection
- Should come with memory capabilities.
- Should have Paper-saving recording
- Should have High level 12-lead ECG analysis
- Meets IEC60601-2-51 international standard for digital electrocardiographs
specifying accuracy and digital filter performance.
2- DISPLAY
- Must have Colour LCD as a Display screen
- Should have ECG waveform: 12 lead ECG
- Display include Patient information, hospital name, recording settings, operation
mode, heart rate, QRS mark, CAL mark, error message, electrode detachment,
noise
3- ECG ACQUISITION
- Should have 12 ECG leads
- Should have Common mode rejection ration: 100 dB
- Should have Input circuit is isolated and protected against defibrillator discharge
- Should have Input impedance is 20M
4- RECORDER
- Should have High resolution thermal array printer
- Should have Printing density 200 dpi (8 dots/mm), 320 dot dot/mm (25 mm/s)
- Should have Number of channels: 3, 4, 6, 12
- Should have Paper speed: 5, 10, 12.5, 2, 50mm/s
- Should have Automatic or manual recording with grid
- Should have Recording data include program type, version, date and time, paper
speed, sensitivity, lead name, filter, hospital name,
- Should have patient information, timing mark, event mark, electrode detachment,
noise
- Should have Recording mode: Manual, Auto, Rhythm, Periodic
5- TROLLEY
Should come with trolley
6- Environment
Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety for Electromagnetic
Compatibility. Or should comply with 89/366/EEC;EMC directive

EQUIPMENT 6
HOLTER ANALYSER SYSTEM
SPECIFICATION
A microprocessor based digital holter, which is small, lightweight, and able to pick up
and record interfaced cardiac activity of ambulatory patients. The unit should able
operate with window based Microsoft system.
FEATURES
-
System should run at least windows 7 and above based software design
User friendly menus and control for faster scanning and editing
Automatic upload with full analysis in less than 60 seconds. The system must be
capable of multiple modes scanning options below:
Prospective or Manual
AutoScan
Should acquire data from 2 or 3 channel recorder for up to 24 & 48 hours or up to
7 days
Should analyse and do reporting of the R-R interval and frequency variation
whereby data can be selected for analysis via optional beat filters and V and SV
ectopic, or from the arrhythmias.
Graphic trending for HR, RR interval, RR Variance, 12 lead ST, SVPB, VPB & Atrial
Fibrillation
Capable of identifying and classifying heart beat : Normal, ventricular, paced
supraventricular, R on T
ST segment analysis should ofer full disclosure or summary tables. Capable of
pacemaker analysis for both arterial and ventricular, and dual pacemaker
detection: capture, over sensing, under sensing
The system should allow simultaneous loading and editing.
Multi-tasking system that allows digitalization, beat and arrhythmias analysis.
Split screen mode allows diferent section of report to be viewed simultaneously.
Histogram for RR interval, SVE and pace spike distribution
Traditional 2- and 3-Channel recording analysis for 24 or 48 hours and up to 7
days: Analysis of Bipolar and Unipolar leads acquired using a traditional 5-wire
patient cable provides beat to beat review and complete presentation of all
arrhythmias and ischemic events. Prints 1-, 2- or 3-channel ECG strips at any
point in time as per users requirement.
Download and Scan Time: Less than 90 seconds.
Color Coded Beat Identification: according to beat types for easy identification.

-
Callipers: Allow measurements of amplitude, time and heart rate.

Report Preview Capability: Facility of editing / reviewing of final reports before
printing. System allows preparation of final reports, including automatic strips,
comments, morphology report, full disclosure and ECG strips.
Full Disclosure Archive: Facility to archive complete full disclosure to external
media such as CD or DVD or any arbitrary drive to create an of-line library of
patient recordings. Archived data is then available to restore from the on-line
library that automatically identifies the storage media disc number or drive
location.
Advanced Algorithm Signal Processing: Algorithms provide superior
accuracy in beat detection, labelling and noise rejection for rapid identification of
rhythm events.
Rhythm Analysis: Rhythm Analysis of Ventricular and Supraventricular singles,
couplets, runs (longest and fastest), bradycardia, tachycardia, atrial fibrillation,
Atrial and Ventricular Pacemaker rhythms, pause, longest RR, RR standard
deviation, and Heart Rate Variability. Percent and total beats in summary and
hourly.
Diary Events: Configurable diary entry labels with automatic patient event stop
during the scan.
Final patient report export utilizing PDF and XML technology.
Optional HL7 or EMR and DICOM Interface capability
COMPUTER HARDWARE REQUIREMENT

-
CPU with Latest Proccessor, Speed and Catch

Minimum 2GB RAM
Minimum Hard-disk Capacity 500GB HDD
Minimum LCD monitor is 23 Touch Screen High Resolution
One Drive of CDR-W
Internal Modem 115Kbps & network card
Preinstalled MS Windows 7 Professional or latest (System Compatible)
Printer Laserjet
Holter Software Installation CD
ACCESSORIES
-
3 channel digital holter recorder x 3 unit

Recorder carrying case x 3 unit
Patient 5 lead electrodes cable x 3 unit
USB Transfer cable x 1 unit
WARRANTY
Minumum Two years warranty against manufacturing defective.
Preventive maintenance (PM) shall provided as per manufacturer recommendation.
TRAINING
On site training is to be provided on the operating and simple maintenance of the
equipment. Service manual and operational manual must be provided.
POWER SUPPLY

240VAC/50Hz.
Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety for
EQUIPMENT 7
EEG MACHINE, WITH VIDEO
SPECIFICATION
-
EEG Amplifier must be IP addressable

EEG amplifier must be connected via CAT5 networking cable
Must be able to initiate impedance check from amplifier
EEG amplifier must have built-in electrode connections
Must have a passive headbox with cable (min. 32 inputs)
Amplifier noise in the recording must be less than 2 uV (microvolts) peak to peak, at
any frequency 0.1 to 100 Hz.
Amplifier sampling rates must be software controlled and adjustable from 125 to 2000
Hz.
Programmable and adjustable montages, recording parameters and recording
notations.
Programming must be fully Windows XP Professional compatible.
Filing system and database management software
Must be capable of archiving patient files to CD, DVD, or Network server.
Must be USB 2.0 compatible.
Must be network ready.
Must provide user in-service for Neurology Technologists.
Must have LED photic strobe capable of 60Hz stimulation
Must be capable of displaying EEG trends such as amplitude integrated EEG (aEEG),
Envelope, Absolute Band Power, Total Power, Burst Suppression Monitoring, Spectral
Edge, Peak frequency, and Spectrogram, during acquisition and review
WARRANTY

TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 8
EMG MACHINE
SPECIFICATION
1- COMPUTER HARDWARE
- Minimum Latest processor
- 4 GB RAM, minimum 500GB harddisk Drive
- Writeable DVD-ROM drive, sound card, keyboard and mouse
- Windows 7 Professional
- Laser printer
- 23" Full Touch HD display
- Mounting bracket for LCD display
- User interface Control Panel

- Mobile cart on castors
2- AMPLIFIER
- Minimum 4 channel input or more
- Input impedance : 200 M
- Noise level < 0.6 Vrms or less at 1 Hz to 10 kHz with input shorted
- CMMR: 106 (Balanced mode), 112 dB (Isolation mode)
- Sensitivity: 1, 2, 5, 10, 20, 50, 100, 200, 500 V/div, 1, 2, 5, 10 mV/div 5%
- Low-cut filter: 0.01, 0.02, 0.05, 0.1, 0.2, 0.5, 1, 2, 5, 10, 20, 50, 100, 200, 500
Hz, 1, 2,
- 3 kHz at 6 dB/oct (20%)
- High-cut filter: 10, 20, 50, 100, 200, 500 Hz, 1, 1.5, 2, 3, 5, 10, 20 KHz at 12
dB/oct
- (20%)
- AC interference notch filter: 50/60 Hz (rejection ratio: < 1/20)
- Amplitude calibration: 1, 10, 100 V, 1, 10 mV (within 5%)
3- AVERAGER
- A/D converters: 16 bits
- Conversion speed: 10 s/channel max
- Analysis time base:
With a list box:0.1, 0.2, 0.5, 1, 2, 3, 5, 10, 20, 30, 50ms/div, 0.1, 0.2, 0.5, 1
s/div
- (within 5%)
- With a keyboard:
i)
to 0.9 ms in 0.1 ms steps (within 5%)
ii)
to 99 ms in 1.0 ms steps (within 5%)
iii)
100 to 1,000 ms in 10 ms steps (within 5%)
- Time base mode:
Individually selected for each channel
- Number of averaging:
1 to 9999
- Artifact reject inhibit range:
1, 2, 3, 4, 5 div on screen or of (No artefact rejection)
4- STIMULATOR COMMON FUNCTIONS
- Trigger modes:
Recurrent, Random, Foot Switch, Signal, External
- Stimulation modes:
Single, Double, Train
- Trigger signal output
Amplitude: 5 V (within 5%)
Duration: 1, 5, 10 ms (within 20%)
5- ELECTRIC STIMULATOR
- Stimulation intensity:
i)
to 100 mA (in 0.1, 0.2 or 1 mA steps)
ii)
2.1 mA to 100 mA: within 5%
- Stimulation pulse duration:
1, 0.5, 0.3, 0.2, 0.1, 0.05, 0.03, 0.02, 0.01 ms
i)
ms to 1 ms: within 10%
ii)
0.05 ms: within 20%
6- AUDITORY STIMULATOR
- Output type: Headphone, Earphone
- Stimulation modes: Click, Tone burst
- Stimulation phase (polarity): Condensation (positive), Rarefaction

(negative), Alternating
Stimulation intensity: 0 to 135 dB SPL in 1 or 5 dB steps (within 2 dB)
Contralateral white noise masking:
0, -10, -20, -30, -40dB or of (no masking) (within 5 dB)
- Click pulse duration: 0.1 to 1.0 ms in 0.1 ms steps (within 5%)
7- VISUAL STIMULATORS
- Stimulation modes:
Pattern reversal. LED goggles, External visual stimulation
- Pattern reversal:
i)
Field format: Full, left half, right half, upper half, lower half, upper left,
lower left, upper
ii)
Right and lower right field
iii)
Patterns: Checkerboard, horizontal bars, vertical bars
iv)
Number of horizontal division for pattern: 4, 8, 16, 32, 64, 128
v)
Display time (duration): 20 to 1000 ms in 10 ms steps
-
8- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety for

EQUIPMENT 9
STRESS TEST SYSTEM, WITH TREADMILL

OPERATIONAL REQUIREMENT
In this system the patient exercises on a treadmill according to a standardized protocol
and the cardiac abnormalities can be studied under stress conditions which we may miss
under resting
SPECIFICATION
1- Should acquire and analyse 12 simultaneous ECG Leads
2- Should have facility for display of all 12 leads real time Rhythm ECG on screen
3- Should have facility of on line storage of patient ECG data. Storage of at least 500
patients on HDD.
4- In addition the storage on floppy drive or CD should be possible
5- Updated medians with elimination of Artifact ectopy and aberrancy in all leads
6- Filters with facility to eliminate Artifact due to respiration muscle/noise, AC
interference, baseline wandering without compromising/distortion in ST segment
changes
7- Should have facility to do the reanalysis of stored ECG report with reanalysis of
the current stress report by changing the measurement point i.e. E, J and post J
points
8- The monitor should display auto comparison of resting versus current lead of
maximum ST depression separately with colour coded protocol, stage, clocks for
elapsed time, total time, Target HR, Treadmill speed & grade, PVC counts/minute,
warning messages & prompts, lead check torso
9- Should have facility for 12 lead resting electrocardiogram with full interpretation
10- System should print comprehensive final report on a minute by minute record of
ST segment changes ST segment trend plot and acceleration of ST segment
11- Display should have facility to amplify a normal gain along with a sample of
resting ECG complex for close test
12- System should be able to provide the real time printing by auto or manual mode
in desired formats. Writer resolution should be thermal 1000 line/sec x 200 dpi for
printing
13- The treadmill should always start from 0 mph and has load capacity of 450 lbs.
And speed range of 0-13.5mph and elevation 0-25% and should have facility to
run the self-calibration programme. Treadmill should have minimum 60" walking
surface.
14- Treadmill should have two stop modes with digital Microprocessor control,
including one patient activated stop mode. The same should be interfaced to the
main analysis system.
15- Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility.
EQUIPMENT 10
NEBULIZER

SPECIFICATION
1- Particle Size
- Shall Designed for continuous use
- Suitable for Hospital, clinic and home use
- Should have Powerful compressor for heavy usage
2- Desk Type Nebulization
- Minimum Output is 1 to 5 microns
3- Maximum Cup Capacity
- 0.4-0.7 ml/min
4- Oscillating Frequency
- 8ml Particles :1-5 micron
- 2.4 MHz approx.
- Including mouth piece , tubes , filters , masks for infant and paediatrics
220v/50hz
EQUIPMENT 11
HEMODIALYSIS MACHINE
SPECIFICATION
1- Machine should have facility for Acetate, Bicarbonate and sequential dialysis
2- Cab be linked to patient data Management System and should be upgradeable to
future development
3- Should have facility for conventional and high flux dialysis
4- Battery backup for at least 30 min to run complete machine with heater supply
5- Should have Na, Bicarbonate and UF profiling
6- Dialysate temp selectable between 35-39 degree Celsius.
7- Variable conductivity between 12-15.
8- Should have dialysate flow 250-800ml/min.
9- Heparin pump with syringe sizes up to 50ml and pump rate of 1-10ml/hr.
10- Stroke pressure operated short term single needle dialysis.
11- UF 0.1-2.5 litre/hr. The in and out fluid circuit must be separated so that there is
no chance of contamination in case of membrane rupture.
12- Treatment parameter should be displayed by graph and digitally both.
13- Should have integrated heat and chemical disinfection.
14- Should have accurate feedback control conductivity mixing technique.
15- Should have drain facility.
16- Should have accurate UF control by flow measurement technique.
17- Extra facilities like blood volume sensor, Bicab select technique and online
clearance (optional)
18- All important data should be present so that the machines can be used anytime
without feeding data every time.
19- Should have automatic test facility.
20- Should have auto on of facility.
21- Should have touch button screen.
22- Easy to service, trouble shoot and calibrate.
23- Machine can be connected to computer to feed all data and trouble shoot and
calibrate.
24- Blood pump rate from 20-500ml/min adaptable to all standard AV blood lines.
25- Audio visual alarms on limit violation of conductivity, blood leak, air leak,
transmembrane pressure alarms, dialysis temp alarms, dialysis can empty alarm,
end of disinfection alarm, bypass alarm, and blood pump stop alarm.
26- Alarm for reverse Ultra filtration.
27- The unit shall be capable of being stored continuously in ambient temperature of
0-50 deg C and relative humidity of 15-90%.
28- The unit shall be capable of operating continuously in ambient temperature of
10-40 deg C and relative humidity of 15-90%.

29- Manufacturer/Supplier should have ISO certification.
30- Shall comply with IEC 60601-2-16 safety requirements of medical electronic
equipment part requirement for HD machines.
WARRANTY
TRAINING
POWER SUPPLY
240VAC/50Hz.
Should have FDA, CE, UL and BIS approved product.
EQUIPMENT 11
HEMODIALYSIS MACHINE
SPECIFICATION
-
Machine should have facility for Acetate, Bicarbonate and sequential dialysis
(isolated UF)
Can be linked with patient Data Management System (Optional) and should be
upgradeable to future software developments
The blood pump should run even in the absence of water or dialysis flow
Should have facility for conventional dialysis with latest microprocessor controlled
technology.
Machine should have one 10 microns filter at water inlet and one bacterial filter
before water going to dialyzer (in built)
Battery back-up for at least 20-30 mins.
Should have Na and UF profiling
Dialysate temperatures selectable between 35 degrees to 39 deg. 3.6 Variable
conductivity setting between 13-15
Should have variable dialysate flow 300-800 ml per minute or more.
Should have facility to show trends curve of all parameter for 15-20 minutes.
Heparin pump with syringe sizes up to 10-20 ml or more with pump flow rate
from 1-10 ml per hour (0.1 increments)
Stroke pressure operated short term single needle dialysis (Optional)
Ultra filtration 0.1 to 2.5 litres/hr. The in and out fluid circuit must be separated so
that there is no chance of contamination in the event of membrane rupture.
Treatment parameter should be displayed both by graph and digitally
Should have integrated heat and chemical disinfections facility.
Should have accurate feedback control conductivity mixing technique.
Should have drain facility.
All important data should be present so that machine can be used anytime
without feeding data every
Should have automatic self-test facility.
Should have auto ON/OFF Facility.
Machine should have TFT screen with soft touch button controls.
Easy to service, troubleshoot and calibrate
Machine can be connected to computer to feed all data and trouble shoot
whenever any problem.
Blood pump rate from 20-500 ml/min adaptable to all standard A - V blood lines
Ability to monitor pulse rate and NIBP with graphic and tabulated trends.

Audio visual alarms on limit violation of conductivity, blood leak, air leak, trans
membrane alarm can empty alarm, end of disinfection alarm, bypass alarm and
blood pump stop alarm.
Alarm for reverse Ultra filtration.
Machine should have real time clearance surveillance for urea & Kt/V to assess
adequacy of dialysis. It should display real time urea clearance, plasma sodium,
current Kt/V and time required to achieve target Kt/V.
Power Supply
Power input to be 220-240 VAC 50 Hz fitted with plug.
On line UPS of suitable rating with voltage regulation and spike protection for 60
minutes backup
Standards, Safety and Training
Should be CE/ UL /BIS approved product
Manufacturer/Supplier should have ISO certification for quality standards.
Shall comply with IEC 60601-2-16 SAFETY requirements of medical electric
equipment Part-2 particular requirements for the safety of Haemodialysis
Comprehensive training for staf and support services till familiarity with the
system.
Should have local service facility or service provider must attend break down call
within 24 hours.
The service provider should have the necessary equipment recommended by the
manufacturer to carry out preventive maintenance test as per guidelines provided
in the service documentation
-
EQUIPMENT 12
STETHOSCOPE (ADULT, PAEDS & INFANT)
SPECIFICATION
1- Should have Chrome-plated.
2- Dual-head chest piece with chest-piece has white diaphragm Complete
with 2 spare ear tips and a spare diaphragm.
3- Size: Adult, Paediatric & Infant
EQUIPMENT 13
RESUSITARE BAG (ADULT, PAEDS & INFANT)
SPECIFICATIONS
1- Hand held silicon type.
2- Main unit consists of :
Pressure regulator with mask and plastic hood.
Face mask for child (3 pieces)
Face mask for adult (3 pieces)
Oxygen reservoir bag with safety valve (1 piece)
3- Oxygen feeding tube (4 pieces) including carrying bag
Specifications : Self inflating bag volume: approx. 1600ml
Oxygen reservoir bag volume : approx. 2600 ml,
Autoclavable Materials: Self inflating bag: semi.
Transparent silicon rubber.
Valve housing: transparent polysulfone Shell of mask: transparent
polysulfone.
Cushion of mask: transparent silicon rubber
EQUIPMENT 14
LARYNGOSCOPE (ADULT, PAEDS &

NEONATE)

SPECIFICATION
1234-
5678-
Stainless steel construction with satin,

Non-glare finish that provides rugged durability.
Both Macintosh and Miller laryngoscope style blades are available.
The Size of Blade are;
iAdult:
2,3 & 4
iiPaeds:
Curve & Straight
iiiNeonate: 0 & 00
Langyngoscope Handle:
iSuitable for Adult, Paeds & Neonate
Satin chrome-plated brass with a knurled finish for a positive grip
Rugged durability and lightweight design
Battery Operated
EQUIPMENT 15
HARMONIC SCAPLE
SPECIFICATION
- Ultrasonic generator
iwith fixed frequency of 55.5 KHz (as per manufacturer
recommendation & specification)
iiwith capable of incising tissue and providing homeostasis
iiiwith minimal thermal injury
ivwith having 5mm instruments/probes/shears for both Open and
laparoscopic surgeries.
vwith minimal 3 discreet audible tone settings possible to indicate
generator status with have an option of reusable HAND ACTIVATION
viwith bilateral switches to change power levels with having
viiwith provision for connecting 2 footswitches for two surgeons to
work simultaneously
viii- with having self-diagnostic mode to detect any problem with
generator, footswitch, transducer or instruments
ixwith a graphical display to enable surgeon/technicians to
understand the problem
xwith have a warning system for a worn out probe/shear/instrument
xiwith error codes for better diagnosis
xiiwith have a vibration range of 50-110 microns (micro meters,m)
for optimal cutting and coagulation(as per manufacturer
recommendation and specification)
xiii- with have an option of using 5mm Laparoscopic/Open Shears with

xivxv-
integrated hand activation for better control

with having shears of variable lengths for diferent surgeries
with having probes with integrated hand activation and ability to
adjust the lengths in order to facilitate better dissection in open
surgeries.
WARRANTY
Minumum Two years Full warranty against manufacturing defective.
Minimal Preventive maintenance (PM) shall provided as per manufacturer
recommendation.
TRAINING
Onsite training is to be provided on the operating and simple maintenance of
the equipment. Service manual and operational manual must be provided.
POWER SUPPLY
240VAC/50Hz.
Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety
directive
System Should have FDA, CE, UL and BIS approved product.
EQUIPMENT 16
REFRIGERATOR, PHARMACEUTICAL
SPECIFICATION
Minimum Capacity required is 1,000 Litre
Internal and External Chamber should be EXPOXY Coated
Temperature Control / Range should be within +2C to +8C and being display in
LED
Temperature Fluctuate is 1C to 2C
Refrigerant is R134A / R407 CFC free
Should have at least 1 door lock and castor
Should have alarm system feature: High Low Alarm, Power Failure, Remote Alarm
Contact
Should have UPS with capacity 3kVA
Standard complied with IEC601 electrical safety and ISO 13485

WARRANTY
recommendation.
TRAINING
Onsite training is to be provided on the operating and simple maintenance of the
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 17
REFRIGERATOR, MEDICAL
SPECIFICATION
Minimum Capacity required is 800 Litre
Internal and External Chamber should be EXPOXY Coated
Temperature Control / Range should be within +2C to +8C
Temperature Fluctuate is 1C to 2C
Refrigerant is R134A / R407 CFC free
Should have alarm system feature: High Low Alarm, Power Failure,
Remote Alarm Contact
Standard complied with IEC601 electrical safety and ISO 13485
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.

EQUIPMENT 18
HEAD LIGHT
SPECIFICATION
Should be use White, xenon-quality light
System Should produce at least 550 hours of Operation time
Unit interface must be Soft, flexible in headband with dual ratchets for superior
comfort and fit
Should have Fiber-optic bundle with layers of protective materials to prevents
fiber breakage
WARRANTY
recommendation.
-
TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 20
HEART LUNG MACHINE
1. GENERAL FEATURES
iProgrammable & Modular System
iiCapabilities for future upgrading
iiiConsole to accommodate 5 pumps
ivIncludes Uninterruptible power supply (UPS)
vBi-directional brushless horse-shoe shaped roller pump
viDisplays Temperature/Pressure
viiAudible and visual alarms
2. TECHNICAL SPECIFICATIONS
iMicroprocessor controlled Single head roller pump with touch-screen panel
is mainly used for arterial blood flow, for suction and venting
iiDouble head roller pump with touch screen panel which can be operated
together
iiiAll roller pumps shall be a direct-drive DC brushless motor type. The
pumps shall be quiet and vibrations-free during operation
ivIncremental encoders (IE) is capable of both fine and coarse adjustments,
audible indication at 0 to 250 rpm
vRotatable pump head can be adjusted in 15 degree increments from -90
deg to +90 deg
viBattery backup time under operating conditions must be at least 90
minutes when fully charge
viiSingle Head Pump
Diameter of pump head raceway : 150mm
Diameter of occlusion roller : 30.5mm
Speed range : 0 to 250 RPM (clockwise, anticlockwise)
Deviation in speed accuracy +/- 1%
Deviation in speed accuracy in case of error +/- 15%
Direction of rotation: Clockwise / Anti-clockwise
Concentricity of Pump Head Raceway 45 deg C
Measuring Interval : +/- 1 - 2 seconds

Accuracy of SAT measurement: in 60 to 100% range : +/- 4% And

in 40 to 59% range : +/- 6%
Accuracy of HCT value measurement: in the 15 to 50% range: +/6%
Accuracy of temp. measurement: in the 25 to 40deg C: +/- 0/6 deg
C (at room temp of approx 23 deg C)
viiiOXYGEN ANALYZER * Oxygen Analyzer & Monitor for the medical industry
Microprocessor based with LCD backlight for easy visual/Large easy
to read display
Alarms if sensor becomes disconnect
Auto Calibration
Battery Test Key
Sensor comes with flow diverter
V mount adapter supplied
Two alarm set points - fully adjustable
ixEssential Components
1 x 4-Pump Console to accommodate up to 5 pumps complete with
built in Emergency Pack (EP Pack) and UPSE battery with
charger/discharger
1 x 5-slot system panel
5 x Control Display Module
3 x Single Roller Pump
1 x Double Roller Pump
3 x Tubing Clamps Variolock
1 x 2-Channel Pressure Transducer with clamps/holders &
connecting cable
1 x Timer
1 x Temperature Module
1 x Level Module
1 x Sensor Module for Bubble Detector sizes 3/8
1 x Cardioplegia Sensor Module
1 x Venous Occluder (Electronic)
1 x Air & Oxygen Blender
1 x Heating Cooling System 3-Channels
2 x Chair for perfusionist
1 x Remote Control (Patient Circuit)
1 x Remote Control (Cardioplegia Circuit)
1 x Adult Blanket/OR Table size 24x 60
1 x Blanket Adaptors
1 x LED Lamp
1 x Integrated In-Line Blood Gas Monitoring
1 x Digital Oxygen Analyzer Monitor with Alarms
1 x Various Tubing inserts necessary for machine operations
1 x Disposable Pads for Level Sensors
3Power Supply
- Power input to be 220-240 VAC 50 Hz fitted with plug.
- On line UPS of suitable rating with voltage regulation and spike protection for
60 minutes backup
4- Standards, Safety and Training
- Should be CE/ UL /BIS approved product
- Manufacturer/Supplier should have ISO certification for quality standards.
- Shall comply with IEC 60601-2-16 SAFETY requirements of medical electric
equipment Part-2 particular requirements for the safety of Haemodialysis
- Comprehensive training for staf and support services till familiarity with the
system.
- Should have local service facility or service provider must attend break down

call within 24 hours.
EQUIPMENT 21
BLOOD GAS ANALYSER
SPECIFICATION
-
Handheld ABG Reader.

It should measure Blood Gas (full parameters) in its addition to measure
Electrolytes. pH, pCO2, pO2, Na+, K+, Ca++, Cl-, Glu, Hct, Lac, and Crea.
Calculated values: cHCO3-, cTCO2, BE(ecf), BE(b), cSO2, cHgb, eGFR, eGFR-a,
AGap, and AGapK
Room temperature test card storage
Internal electronic QC and automated internal QC check
Critical result reporting
Test Card and patient ID barcoding
Transmit results securely in real time
Should display all results in print out and c/w thermal printer
Analyzer with memory of storing patient data/result
WARRANTY
recommendation.
TRAINING

EQUIPMENT 22
INFUSION PUMP, VOLUMETRIC
SPECIFICATION
-
The equipment should have Roller type Peristaltic pump /Volumetric pump
technology for delivery of IV fluids and blood/blood products ranging
Volume delivery is 0-9,999ml
The Equipment should have high levels of safety from air embolism by
integrating at least two ultrasonic air detection sensors.
Heating process should be done by an electromagnetic induction heating system.
The equipment should have the facility to automatically purge air for removal of
any outgassed air to prevent it from entering the patient line. No manual process
should be involved.
The equipment should have a line pressure control sensor for restriction of flow in
case of line occlusion immediately and stop the delivery of fluids for patient
safety.
The equipment should have an internal rechargeable battery backup.
Consumables should be universal for all flow.
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.

EQUIPMENT 23
INFUSION PUMP, SYRINGE
SPECIFICATION
- The equipment should have plunger type
- Volume delivery is 0-9,999ml
- The equipment should have operator controlled Bolus infusion key for rapid
response in critical situations.
- The equipment should have a line pressure control sensor for restriction of flow in
case of line occlusion immediately and stop the delivery of fluids for patient
safety.
- The equipment should have an internal rechargeable battery backup.
- Should have compatible syringe sizes
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 24
PULSE OXIMETER
SPECIFICATION
- Display LCD, Backlight illuminated.
- Parameters and waveform displayed SpO2, pulse rate
- SPO2 range 60-100%
- Accuracy of SPO2 -3%
- Pulse rate range should be 30-240 bpm
- Audio-visual Alarms- high/low SpO2 and pulse rate, sensor of, sensor failure, low
-
battery.
Alarm override facility.
RS 232C Interface for data communication (as per manufacturer design)
Battery back-up operating minimum up to time 5 hours.
WARRANTY

recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 25
CARDIOTOCOGRAPHY (CTG MACHINE)
SPECIFICATION
-
Cardiotocograph (CTG) machine wide TFT- color LCD screen for Fetal Heart Rate,
Uterine contraction & fetal movement.
It should have Twin Fetal Monitoring system
LCD Screen should be tiltable & rotatable. It should have display modes of Trend
mode, Number mode & Graph mode.
It should have alarm functions in all movement
It should have facility to increase / decrease / mute alarm sounds
It should have Automatic track & hold facility
It should have high sensitivity less than 1 MHz FHR upper limit should be 130 240 BPM & lower limit should be 30 -150 BPM
It should have Fetal Heart Rate & Uterine pressure
It should have automatic and manual fetal movement detection
It should have in built thermal recorder with A4 size
It should have battery back up
It should have a built-in memory to save patient graph data.
Should be supplied with trolley.
Should be supplied with standard accessories
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.

EQUIPMENT 26
ELECTROSURGICAL UNIT, GENERAL

PURPOSE
FUNCTIONAL REQUIREMENTS
The unit is intended for use in cutting and coagulation of tissues in operating theatre.
GENERAL REQUIREMENTS
- The unit shall be designed to perform monopolar and/or bipolar electrosurgery.
- The unit shall have the following mode of operation:
a.
Pure Cutting
b.
Coagulation
c.
Blend Cutting
d.
Bipolar coagulation
-
The unit shall be compact, portable and water resistant.

The unit shall be designed to activate the high frequency generator by means of
finger switch or footswitches.
The unit shall be equipped with a digital display indicating estimated delivered
output power.
The unit shall be capable of monitoring the contact impedance between the patient
and patient dispersive-electrode and shall prevent ESU output activation if the
contact impedance rises above the manufacturer's preset value.
The unit shall be equipped with dispersive-electrode cable continuity monitor that
prevent ESU activation if the cable breaks or disconnected from either the ESU or
the dispersive electrode.
The unit shall be designed with an isolated output capable of eliminating the risk of
burns to the patient that may come in contact with grounded object.
The unit shall be able to use both adhesive return electrode and non-adhesive type
i.e under-body gel pads on patient.
The unit shall be capable of using any brand of diathermy pencil / electrodes.
The unit shall be equipped with automatic self-diagnostic program upon start-up. It
shall continually monitor, detect and indicate defects and malfunctions.
The strain relief for the line cords and footswitch cables should be durable
and able to withstand a strong pulling force.
Front-panel controls should be visible to the user and easily identifiable and
clearly marked
If an alarm is silenced, a visual display shall indicate clearly which alarm is
disabled.
The unit shall be equipped with visual and audible indicator peculiar to the
mode of operation
POWER REQUIREMENT
-
The unit shall operate directly from a 230V 10%, 50 2 Hertz,

-
All accessories shall be fully integrated, with a single 13A moulded

construction power plug.
The unit shall be protected from transient power disruptions during use. The
disruption shall not afect the performance of the unit.
The unit shall be equipped with self-tripping circuit breaker for protection against
overload.
SAFETY REQUIREMENTS
- The construction of the unit shall ensure a sufficient degree against safety hazards
caused by overflow, spillage, leakage, humidity, ingress of liquids, cleaning,
sterilisation and disinfection.
- The enclosure shall be secure and provide adequate protection against moving and
electrically energized parts
- Switches and controls should be protected against penetration of fluids.
Switches and controls shall be protected against accidental setting changes.
The controls (i.e. switches, knobs, etc.) should be visible and clearly identified,
and their function should be self-evident.
Device design
should prevent
misinterpretation of displays and controls settings.
The unit should resist tipping over during use and transport.
The unit shall have no sharp edges.
Connections shall be secured to resist accidental disconnection.
Mechanical electric and pneumatic terminators, connectors, sockets and solder
joints shall be designed to prevent fluid penetration, incorrect connections and
mismatch of fitting and couplings
CERTIFICATION & STANDARD
- The system shall fully conform to the following (or equivalent) :
a.
IEC / EN 60601-1, General safety requirements for medical electrical

equipment;
b.
IEC / EN 60601-1-2 , Standard for Electromagnetic Compatibility
Requirements and tests;
c.
IEC / EN 61000-4-x series, Safety requirements and tests for
Electromagnetic compatibility, Immunity;
d.
IEC / EN 60601-2-2, safety requirement for High Frequency Surgical
Equipment
e.
IEC / EN 60529 (1989), Degrees of protection provided by enclosures (IP
code).
f.
Particular requirements for safety and performance of the tendered
Article(s);
g.
FDA clearance.
TECHNICAL REQUIREMENTS
-
The output power display should be within 20% of the actual power delivered in a
manufacturer-specified load resistance of 100 to 1,000 unless the operator's
manual contains a diferent value.
Maximum output power for 100 to 500 rated load:
a.
b.
c.
d.
e.
Cutting
Blending
Coagulation
Bipolar coagulation
Output frequency
:
:
:
:
300 watts
:
200 watts
120 watts
80 watts
400 kHz
Maximum line frequency source leakage current from electrodes shall be less than
10 microamperes.
Maximum line frequency leakage current from chassis shall be less than 100

-
microamperes
Maximum line sink leakage current when 230V, 50 Hertz, Alternating Current is
applied across either electrode or ground shall be less than 100 microamperes.
Maximum high frequency leakage current from either electrode shall be less than
150 microamperes.
ACESSORIES
- All standard accessories required for the normal operation, shall be listed with
itemised prices
and included in the unit base price.
- The standard accessories shall include the following:
a
b
c
d
e
f
g
Single used Hand switch;

Monopolar Footswitch
Bipolar Footswitch;
Monopolar adapter;
Patient return electrode pad;and
Mobile cart.
All other accessories, cables, connectors and consumables shall be included
for the safe and smooth operation (full functional) of the unit.
WARRANTY
recommendation.
TRAINING
EQUIPMENT 27
OPEN CARE RESUSITARE
OPERATIONAL REQUIREMENTS
Complete system with cart and oxygenation facility is required.
TECHNICAL SPECIFICATIONS
-
Essential parts: Cart & bassinet Warming system with controls & alarms.
Examination light
Storage space- 2 sliding drawers below bassinet 2 platforms
Cart: Should swivel on 4 wheels with foot operated., 2 front lockable wheels.
Bassinet : 1 fixed and 3 movable transparent side walls :Portion above X-Ray
cassette holder radiolucent.

Mattress- Bassinet tilt in steps Trendelenburg or reverse Trendelenburg
Warmer module swivel
Warming systems- Modes :Manual & skin. Manual mode :Adjustable in steps from
zero to 100
Skin mode - Method : Flexible, unbreakable skin temperature probe Set point
range : 34 38 degrees C. Skin temp variability at Temperature equilibrium :+
0.2 degrees C
Skin temperature display- Accuracy : + 0.2 degrees C. Type : digital LED with 0.1
degree resolution. Correlation of displayed And actual skin temp Silence/ Reset
switch : To silence the alarm & reset set point.

-
Alarms
iProbe failure
iiHeat failure
iiiHigh and low temperature
ivPower failure
vSystem failure
Examination light : Illuminance 100 foot candles at mattress center
Storage space : 2 drawers, preferably covered and sliding
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 28
PHOTOTHERAPY UNIT
SPECIFICATION
-
Phototherapy chamber of 18 UVA+18 NB UVB tubes designed for providing even
irradiation of the body in the treatment area.

UV chockes must be provided to provide long life to the tube light and cooling
fans for efective cooling of the unit.

Body to be of a metal which is rust free so as to ensure long rust free life of the
unit.
Automated and/or mechanical safety mechanism to prevent excess irradiation to
the patients so as to avoid/prevent burns etc.

Electrical leakage circuit tripper/breaker in each panel to ensure maximum safety
of the patient.
Open top unit to ensure maximum ventilation and prevent claustrophobia.
Black UV Goggles and Eye pads cover (3 pairs each for adult and 3 pair for
children ) as protective
WARRANTY
recommendation.
TRAINING
POWER SUPPLY

240VAC/50Hz.
EQUIPMENT 30
INCUBATOR
SPECIFICATION
iiiiii-
Continuous bed tilt up to 8 on either sides

Head end raise facility with auto lock.
Both visual and audible alarms for
Patient and control and high / low temperature alarm.
Air circulation / probe / system / power failure alarm.
Humidity control alarm.
Facility to display and trends of temperature information on compatible monitors
with other physiological parameter

With caster wheel with swivel in all directions and with front lockable wheels. Two
shelves cabinet with door.

Patient control (Servo) mode 35 deg-37 deg C. and Air Control (Manual mode)-
20 deg C o 39 deg C.
Air velocity less than 10 cm/sec with inner wall.
Temperature variability less than +/-0.2 deg C. and Temperature resolution 0.1
deg C
Average oxygen input concentration range 5-15 liters/min or 25-70%.
Humidification adjustable electronically with digital display. Standard: 10-80%
dependent on nursery environment and incubator temperature setting.

Double wall canopy with Six hand ports with elbow operated flaps with separate
ports for tubing.

-
Servo control for Oxygen with integrated monitoring

Air filter :- 0.3 micron
Mattress should be radiolucent
2 drawer storage facility and two platforms for keeping monitors
WARRANTY
-

recommendation.
TRAINING
- Onsite training is to be provided on the operating and simple maintenance of the
POWER SUPPLY
- 240VAC/50Hz.
- Suitable battery backup for 30 minutes
- System should have FDA, CE, UL and BIS approved product.
EQUIPMENT 31
INCUBATOR, TRANSPORT
SPECIFICATION
iiiiii-
Continuous bed tilt up to 8 on either sides

Head end raise facility with auto lock.
Both visual and audible alarms for
Patient and control and high / low temperature alarm.
Air circulation / probe / system / power failure alarm.
Humidity control alarm.
Facility to display and trends of temperature information on compatible monitors
with other physiological parameter

With caster wheel with swivel in all directions and with front lockable wheels. Two
shelves cabinet with door.

Patient control (Servo) mode 35 deg-37 deg C. and Air Control (Manual mode)-
20 deg C o 39 deg C.
Air velocity less than 10 cm/sec with inner wall.
Temperature variability less than +/-0.2 deg C. and Temperature resolution 0.1
deg C
Average oxygen input concentration range 5-15 liters/min or 25-70%.
Humidification adjustable electronically with digital display. Standard: 10-80%
dependent on nursery environment and incubator temperature setting.

Double wall canopy with six hand ports with elbow operated flaps with separate
ports for tubing.

Servo control for Oxygen with integrated monitoring
Air filter :- 0.3 micron
Mattress should be radiolucent

-
2 drawer storage facility and two platforms for keeping monitors

Come with Trolley
WARRANTY
-

recommendation.
TRAINING
POWER SUPPLY
- 240VAC/50Hz.
- Suitable battery backup for 30 minutes
EQUIPMENT 32
INFANT WARMER
SPECIFICATION
iiiiii-
Temperature control:
Range 30-38 C
Skin range 25 42
Increment 0.1
Display Digital
Control Unit (to be supplied with.)
Automatic heat control type
Set point mechanism
Heater Indicator.
Alarms (Audible and Visual)
High air temperature
Sensor disconnect
Power Failure
The warmer should include:
Self- check features
Breaks for casters
Skin sensor
Protection against breaks and bursts of radiant and light source
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.

EQUIPMENT 33
FETAL DOPPLER
SPECIFICATION
Handheld and easy to use
Accurate FHR detection and LCD display
Auto counting
Built-in speaker
Automatic switch-of
Battery operated
WARRANTY
recommendation.
TRAINING
EQUIPMENT 34
EXAMINATION LIGHT (HIGH END)
SPECIFICATION
Colour temperature to be between 3,000 and 5,000 K; shadow less
Maximum illumination level at 1m distance to be at least 30,000 lux- 50,000 lux
Colour rendering index to be 93 or greater
Minimum bulb life required 1,000 hours (incandescent type) or 20,000 hrs (LED
type)
Field diameter required 16cm, field depth required 50cm
Focal length required 65 cm
Heat to light ratio to be 6 mW/m2.lx
Brightness control to allow full adjustment from zero to maximum illumination
Bulb voltage and type to be clearly labelled on external body
Replacement bulbs to be locally available
Front panel to include power switch and battery state indicator
Automatic switching to battery power in the event of power failure
WARRANTY
-


recommendation.
TRAINING
POWER SUPPLY
- 240VAC/50Hz.
EQUIPMENT 35
EXAMINATION LIGHT (LOW END)
SPECIFICATION
-
Colour temperature to be between 3,000 and 5,000 K; shadow less

Maximum illumination level at 1m distance to be at least 60,000 lux- 70,000 lux
Colour rendering index to be 93 or greater
Minimum bulb life required 1,000 hours (incandescent type) or 20,000 hrs (LED
type)
Field diameter required 16cm, field depth required 50cm
Focal length required 65 cm
Heat to light ratio to be 6 mW/m2.lx
Brightness control to allow full adjustment from zero to maximum illumination
Bulb voltage and type to be clearly labelled on external body
Replacement bulbs to be locally available
Front panel to include power switch and battery state indicator
Automatic switching to battery power in the event of power failure
WARRANTY
-

recommendation.
TRAINING
POWER SUPPLY
- 240VAC/50Hz.
EQUIPMENT 36
RIPPLE MATTRESS
SPECIFICATION
-
Alternating pressure mattress with support area of 1720MM X 860MM.

To contain 14 air cells with variable geometric section 83MM X 14MM. The
material to contain an anti-bacterial agent.

To have a reinforced base sheet membrane with tucks apron, removable cells and
protective cover.
The compression pump to have a built in equalizing device to prevent over
inflation.
Cycle time to be 10 minutes, to have a low-pressure indicator.
6.To be supplied in a plastic case with handles for easy storage complete with
five spare Cells

WARRANTY
-

recommendation.
TRAINING
POWER SUPPLY
- 240VAC/50Hz.
- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety
directive
EQUIPMENT 37
VENTILATOR, PORTABLE
SPECIFICATION
-
Should be microprocessor controlled, portable, light weight.

Should operate with main electric supply as well as with battery.
Should be able to work both with cylinders and pipeline, connectors and highpressure tubing of appropriate length to be supplied
Should have turbine/piston- technology for supplying air- oxygen mixture.
Should have following modes of ventilation CMV, Assist-control, PS-PEEP
Audio-visual alarms for:
iLow supply pressure
iiHigh/low airway pressure
iiiLeakage/disconnection
ivPower failure
vApnea
viLow battery
Should have following settings
iTV 50 1500ml
iiPEEP/CPAP & PS
iiiRR up to 40bpm
ivI: E ratio 1:3 to 2:1
vFiO2 40 100%
Rechargeable batteries.
Should fix, on rails of transport trolley and on stand with wheels. Two sets of
reusable silicon ventilator circuits.
WARRANTY
recommendation.
TRAINING

POWER SUPPLY
240VAC/50Hz.
EQUIPMENT 38
OPERATING MICROSCOPE, ENT
SPECIFICATION
FLOOR
i.
ii.
iii.
iv.
v.
STAND
Roll able heavy Floor Stand with locking device.
Magnetic system for balancing lock and release of magnetic breaks.
Manipulation to any position with locking for trouble free operation
LCD display of function and parameters, individual programming for diferent
Surgeons.
MICROSCOPE BODY
i- Motorized Zoom Magnification system with apochromatic optics
ii- Magnification 2.1X to 21.5 or better activated by hand grip and foot control with
manual
iii- Override
iv- Eye piece 12.5X
v- Internal Motorized fine focusing system, activated by hand grip and foot control
vi- continuously
vii- Adjustable working distance from 200 mm to 500 mm or more without exchange
of
viii-Objective lens, manual override, integrated continuously variable illumination
field spot
ix- size
x- integrated beam splitter with two additional output inbuilt for connection of
observation
xi- device and video
xii- Stereo co observation system for assistant surgeon/ teaching purpose
xiii-Future up gradation to XY module
BINOCULAR TUBE
i- 180 Degree or more tilt able binocular tube with focal length f= 180 mm or more
ii- Graduated knob for continuous adjustment of inter- papillary distance from 55
mm to 75mm
EYE PIECE
i- Pair of wide field push in eye piece 12.5 X with magnetic locks
ii- Diopter setting from -8 D to +5 D
ILLUMINATION SYSTEM
i- Coaxial xenon illumination minimum 180 Watt with a backup lamp changer Xenon
or halogen bulb
HANDGRIPS
i- Easily removable handgrips with adjustable keys for zoom and focus
ii- Four freely programmable keys for setting illumination intensity, controlling the
video camera
FOOT CONTROL PANEL

i-
Control keys for zoom, focus, movements and light intensity
DIGITAL VIDEO CAMERA SYSTEM

i- 3 CCD advanced digital camera with adapter
ii- LCD monitor compatible with camera- 21 inches
iii- Compatible recording device preferably a digital one with USB Port.
iv- Above microscope should be compatible for LASER use
v- Compatible CVT should be supplied for protection from voltage fluctuation
WARRANTY
recommendation.
TRAINING
POWER SUPPLY
240VAC/50Hz.
EQUIPMENT
CAMERA SYSTEM, LAPAROSCOPY

CAMERA SYSTEM, ARTHROSCOPY

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TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

AUDIOMETER, TESTING BOOTH

* As per recommendation by Act

1200 W x 950 L x 2100 mmH

Double glazed observation window

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

Available and delivered energy

- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

ECG MACHINE, 12 CHANNEL

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

HOLTER ANALYSER SYSTEM

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

Callipers: Allow measurements of amplitude, time and heart rate.

Final patient report export utilizing PDF and XML technology.

Optional HL7 or EMR and DICOM Interface capability

COMPUTER HARDWARE REQUIREMENT

CPU with Latest Proccessor, Speed and Catch

3 channel digital holter recorder x 3 unit

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

EEG MACHINE, WITH VIDEO

EEG Amplifier must be IP addressable

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

8- Meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of Safety for

STRESS TEST SYSTEM, WITH TREADMILL

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

STETHOSCOPE (ADULT, PAEDS & INFANT)

RESUSITARE BAG (ADULT, PAEDS & INFANT)

LARYNGOSCOPE (ADULT, PAEDS &

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

Stainless steel construction with satin,

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

integrated hand activation for better control

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

HEART LUNG MACHINE

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

Accuracy of SAT measurement: in 60 to 100% range : +/- 4% And

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

BLOOD GAS ANALYSER

Handheld ABG Reader.

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

INFUSION PUMP, VOLUMETRIC

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

INFUSION PUMP, SYRINGE

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

CARDIOTOCOGRAPHY (CTG MACHINE)

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

ELECTROSURGICAL UNIT, GENERAL

The unit shall be compact, portable and water resistant.

The unit shall operate directly from a 230V 10%, 50 2 Hertz,

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

All accessories shall be fully integrated, with a single 13A moulded

IEC / EN 60601-1, General safety requirements for medical electrical

TECHNICAL SPECIFICATION OF MEDICAL EQUIPMENT

Single used Hand switch;

OPEN CARE RESUSITARE

cassette holder radiolucent.