ANAESTHESIA DEPARTMENT

36 Pages·2013·0.15 MB·English

ANAESTHESIA DEPARTMENT
SPECIFICATION OF ANAESTHESIA WORK STATION
- O , N O & Air flow meter
2 2
- Should have facility to give low flow anesthesia
- Should have safety features for Oxygen failure alarm, minimum Oxygen flow & hypoxic
guard.
- Should have integrated ventilator with at least pressure support, PEEP, FiO with battery
2
backup
- Should have integrated multimonitor with battery backup with following parameters:
(a) Pulse oximetry-with one adult & one pediatric probe
(b) Capnography- Side stream type with inspired & Et CO ,inhalational anesthesia
2
agent monitoring with MAC values & graphic representation of Et CO
2
(c) ECG Monitoring- 5 leads ECG
(d) Temp. monitoring- with one skin & one rectal probe
(e) NIBP- with one adult, one pediatric & one neonatal cuff
(f) Provision for invasive BP monitoring
- Should have closed circuit with circle absorber
- Proper space for keeping drugs & disposables
- Adequate drawers to keep accessories
- Silicon reusable circuits- one adult & one pediatric
- Machine should be supplied with suitable UPS
- Should have FDA/CE approval
Accessories:
1. Moisture trap for EtCO module=20
2
2.Capnograph lines=30
SPECIFICATIONS OF CARDIAC MONITOR DEFIBRILLATOR AND RECORDER
 Should be Biphasic Defibrillator, monitor with recorder .
 Should have facility for automatic external defibrillator (AED) and Manual Defibrillator.
 Should have facility for 3/5 lead ECG Monitoring and Synchronized Cardio version.
 Should have Adult and Pediatric Paddles.
 Should have ten second charging time for maximum energy.
 Built in charger.
 Charging should be through paddles also.
 Should work on 210-230 volts.
 Battery back up for discharges.
 Multiple viewing angles for clear visibility.
 Should have built in Strip Printer.
 Should have facility for printing critical events.
 Facility for in built SpO2 monitoring .
 User selectable low and high Heart Rate alarm.
 Low SpO2 alarm.
 Facility for in built Pace-Maker (non-Invasive)- demand and non-demand type pacing.
 I.E.C.or equivalent safety certification.
 FDA / CE or equivalent certification.

Essential Accessories
1. Trolley: Good quality rust proof material with castors and break, with one drawer to keep
accessories.
2. SpO2 Probe Adult and Pediatric.
3. Pacing Pads.( one box of 10 nos.)
SPECIFICATION OF MULTIPLE VITAL SIGN MONITOR (MULTIMONITOR)
1. It should have modular design with colour coded interchangeable modules.
2. It should have valid FDA approval and CE certification
3. It should function on AC mains and should have rechargeable internal battery of more
than 2 hrs capacity.
4. Monitor should have port for connectivity to central nursing station and hospital local
networking system.
5. It should have bright and highly visible TFT screen display of 14” to 18”.
6. Should have capability to monitor at least 6 real time wave forms along with related
numerical parameters on a single configurable screen.
7. It should monitor SPO2, pulse rate, ECG, NIBP, Respiration, 2 temperatures, 2 invasive
pressures, Respiratory gas monitoring for E+CO2 with provision of suitable audio visual
alarms.
8. It should have capability to monitor the above parameters in adult, pediatric and patients.
9. The size of numeric and wave forms should be adjustable.
10. Colors of display of various parameters should be interchangeable.
11. It should have facility for monitoring 12 lead ECG including 12 lead ST segments
through 5 lead ECG cable.
12. It should have a minimum of 24 hours graphical, tabular trending facility.
13. It should have advanced multilead arrhythmia analysis capability.
14. Standard accessories and peripherals for monitoring the parameters mentioned in Para 7
audit, pediatric and patients should be provided.
BLOOD BANK
SPECIFICATION OF AUTOCLAVE
1) Electrically operated ( 220 V- 240 V)
2) Vertical type
3) Should be double walled
A) Inner wall made up of S.S.
B) Outer wall made up of M.S. / S.S.
4 ) Size 550mm x 350 mm ( approx )
5 ) Lid should be made up of stainless steel & provided with tightening device
6)Should have pressure gauge, water level indicator , steam release valve &
safety valve & drain for emptying the Autoclave .
7)Joint less Gasket in one piece
8)Working pressure 10psi to 20psi .
9)To be supplied with cord, plug & stainless steel basket .
10)Should have a pedal lifting arrangement to lift the lid.
SPECIFICATION FOR BLOOD BANK REFRIGERATOR
1. Capacity of 500-600 Liters or more.
2. Capacity to hold Minimum of 300 blood bags of 450ml.
3. External Construction-- MS
Internal Construction –SS
4. Should have 4-6 fully extendable, solid bottom, stainless steel drawers with smooth
sliding and locking system and drawer dividers.
5. Lockable castors
6. Should have adjustment for uneven bases.
7. CFC free insulation
8. temperature range+2 to +4o C + 1o C.
9. Positive forced air circulation to maintain temperature uniformity in all the areas of the
cabinet
10. CFC free hermetically sealed compressor
11. Capable of operating at ambient temperature upto +43o C
12. Automatic defrost
13. Automatic condensate removal with no requirement for separate drainage lines
14. Heated dual pane insulated glass door with safety lock and key
15. Interior fluorescent light
16. Large and clear digital display for set/run parameters.
17. Weekly, circular, inkless, temperature Chart Recorder.
18. Independent microprocessor temperature controller
19. Independent alarm and monitor system with battery backup of apprx. 4 hours,
Audio-visual alarm for high and low temperature, power failure, door open and sensor
failure
20. Temperature recorder probe ,independent from other probes for connection to data
logger
21.220-240 volts/50Hz
22. Suitable voltage stabilizer compatible with the equipment to be provided.
23. Should be CE/FDA/BIS approved
24. Electrical safely certification
25. User/Technical/Maintenance manual to be provided in English
26. Logbook with instruction for daily, weekly, monthly, quarterly maintenance checklist, the
job description of hospital technician and company service engineer should be clearly spelt out.
BLOOD COLLECTION MONITOR

• Should have complete flow cut-off when collection weight is reached.
• Should have battery operation for mobile use
• Should be display collection start & finish time.
• Should be suitable for mobile environments.
• Should automatic tare to zero for the bag weight
• Should calibrates in less than 15 minutes
• Should have donation time upto 20 min
• Power Consumption should be max 10 VA
• Should have48 hs. Battery backup,
• Accuracy - <1% of max weight +/- 1 ml
• Measuring range should be up to 999 ml.
• Should have alarms for – Low Battery, under weight, over weight, Taring Error, set up
Error, Motor Error, Abnormal Blood flow, Time Over.
• Should have option for Barcode reader.
• Real time flow rate indicators assist phlebotomists without alarming donors...
• Weight should have approx. 5.5 kg.
• Should work at AC supply of 220-240V 50-60Hz.
• Should be FDA / CE or BIS approved product
SPECIFICATION FOR -30OC DEEP FREEZER
1. Should be of 4-6 drawers with 300 to 380 L capacity and a microprocessor temperature
controller with build in alarms monitor, front loading.
2. Should have adjustable temperature range of -10O to -40O C
3. Electrical refrigeration system defrost can be programmed to actual time desired,
allowing defrost cycle to run automatically during low use period.
4. Controller to be equipped with a temperature probe mounted in the system.
5. Digital calibration offset adjustment for controller calibration.
6. Four inch seven day circular chart recorder with following features:
a) Inkless ,pressure –sensitive chart paper with range of -50O C to 0O C
b) Electronic drive mechanism for consistent results.
c) Battery backup insures continuous operations.
d) Touch button controls for chart changes and calibration.
e) Power status indicator.
7. Refrigeration system:
a) Heavy duty, air cooled refrigerated system
b) Non-CFC, Commercially Available Refrigerant.
c) Internal evaporator is standard.
d) Internal evaporator fan(s) shut off during door opening.
e) Forced air circulation maintaining chamber uniformity of + - 1O C and provide
quick recovery.
f) Balance flow refrigeration system eliminate defrost cycle and maintains constant
temperature.
8. Cabinet :
a) Exterior, interior and door handler(s) made from galvanized steel with bacteria –
resistance powder coating.
b) Superior engineered frame for maximum rigidity.
c) Contoured door handling.
d) Non CFC foamed urethane insulation.
e) Heated, dual-pane, insulated glass door(s) remove fogging and condensation.
f) Standard key lock.
g) Drawers are stainless steel to guard against rust and corrosion.
h) Swivel locking caster
9. Drawers:
a) Solid stainless steel pulls out drawers.
b) Adjustable SS shelves
c) Easy access to inventory with fully extendable drawer slides.
10. Audio visual electronic alarm system independent of power supply
11. Suitable UPS for minimum of 30 minute backup
12. Overcurrent breaker
13. Operable continuously at ambient temp. of 100 to 450 C
14. FDA, CE or BIS approved product
TECHNICAL SPECIFICATION OF FULLY AUTOMATIC WALK AWAY
ELISA/IMMUNOASSAY
• ELISA System is required to Read the color change in ELISA Plates and Strip, automatic
programmable washing & dispensing system high throughput.
• Fully automated ELISA system with 4 microplates assays modular design for reader,
washer & incubators.
• Integrated robotic sample processor. Should have an open system for different makes kits
& manual over ride.
• Predilution facility should be presented.
• Random access, provision for multiple assays.
• Parallel sample pipetting should be present.
• 6 filters with a minimum range of 400-700 nm are required.
• Minimum 12 measurements.
• 16 ways manifold washing with minimum 4 wash channels.
• Volume of wash liquid dispensed variable & intervention.
• Residual volume/ well should be <2µl.
• User friendly software with option for manual intervention.
• Temp. range - room temp to 45 deg C +/- 1⁰ C.
• Plate incubator
• Liquid & clot/foam/bubbles detection should be present.
• Color monitoring check should be provided
• There should be no carryover of sample
• Password protection to prevent unauthorized person’s access to software.