Technical Specifications

Package No:-COVID(GR)-2018
Procurement of “Respiratory Equipment”
(Lot-1 & Lot-2)

Lot -1
SL Description of Item
1. CPAP
Continuous Positive Airway Pressure (CPAP)
1. General description: Should maintain continuous positive pressure in airway for
adult and pediatric use at high flow rate.
2. Features:

 User interface to be easy to operate, numbers and displays to be clearly visible.

 Inspiration trigger for auto start.
 Leakage compensation capability.
 Inbuilt heated humidifier
 Noise level to be less than 35 dbA at mid pressure range.
 In-built air compressor.
 All parts withstand high-disinfection procedures.
 Pressure ramp option that starts prcssure at low level and slowly increases over a
period

3. Technical Specification:
3.1. Display:
 Should have 3" or more LCD/LED/TFT display.
 Displayed Parameters: Pressure [cmH20], Fi02 [%], Flow, Air leak [%],Temperature
(T) etc.

3.2. Operation mode: Continuous, hospital use.

3.3. CPAP generator:
 Pressure setting from 4 to 20 cm H2O or more, adjustable in 4 steps or more.
 Ramp duration: Automatic, 0 to 45 minutes or more
 Should deliver the intended pressure constantly and accurately
 Easy to clean/sterilize
3.4. Air Oxygen Blender:Fi02 concentration should be adjustable (21-100%) and accurate
3.5. Humidifier:
 Should automatically regulate the required temperature
 Humidifier setting temperature should be 35 to 65 °C or wider, in 4 or more steps
 Should be a closed system for filling up water
 Should have ports for heater wire as well as temperature probe
 Should display the chamber temperature and temperature at the patient end.
3.6. Patient circuits:
 Should have the option of using both disposable and reusable circuits
 Air hose length should be 6 ft.
3.7. Data Storage: Should have the data storage and data transfer facility.
3.8. Alarm:
 High/Low Temperature
 Breathing circuit disconnection
 Lack of water
 System failure
  Power failure
 Low battery etc.
3.9. Battery backup: Should have inbuilt battery back-up for at least 60 min.
3.10. Safety Features: Limiting the delivered pressure in the event of an occlusion
etc.
3.11. Portability: Mounting tray and support stand with at least 2 castors fitted with breaks.
3.12. Power Supply: Power input to be 220;240 VAC, 50 Hz fitted with standard plug.
3.13. Accessories: All standard accessories of the offered item must be provided with the
following.
 Inlet bacteria filter, if applicable -05 nos
 Expiratory filters high efficiency - 05 nos
 Nasal mask for adult, with tubing- 04 nos
 Nasal mask for pediatric, with tubing -02 nos
 Oral mask for adult, with tubing - 04 nos
 Oral mask for pediatric, with tubing -02 nos

4. Quality Standards & Safety:

 The offered item should be US-FDA/ EU-CE / JIS) approved product (EU-CE should
be from notified body), certificate of the offered item must be submitted with the offer.
 Brand and model must be engraved/embossed/printed on the machine (sticker
not acceptable).
 Offered model should be brand new, latest model/version and from current
production line not before 2020, a declaration certificate from the manufacturer must
be submitted with the offer. Discontinued product will not be acceptable.

5. Warranty , Spare parts Availability & After Sale Service

 Three (03) years comprehensive warranty with all spare parts and accessories
(without consumables) after the date of installation & commissioning (functioning).
 Availability of spares parts must be for 5 years after the date of installation
& commissioning (functioning).
 The service should be provided by supplier/local agent and should have local
service facility. 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/maintenance manual. The repair /maintenance
work have to carry out within 24 hours after getting request from user.
6.Installation: Installation and commissioning (functioning) by trained engineer should be
completed at earliest and reports must be submitted to CMSD in prescribed format.

7.Documentation:

 Catalogue/data sheet must be submitted with the offer.

 List of the consumables, standard accessories & parts with the price for 5
years of the offered item must be submitted with the offer.
 One set user manual for each machine should be provided during supply of
the equipment (photocopy not accepted).

Lot-2
2. BiPAP
Bi-Level positive airway pressure unit (BiPAP)

1. General description: Should maintain continuous Bi-Level positive pressure in airway for adult
and pediatric use at high flow rate.
2. Features:
 Maintains continuous positive pressure in airway at high flow rate
 User interface to be easy to operate, numbers and displays to be clearly visible.
 Should provide a higher positive pressure airway upon inhalation than upon
exhalation.
 Built-in air compressor.
 nbuilt heated humidifier
 Noise level to be less then 35 dBA at mid pressure range.
 Expiratory relief features that reduce the pressure slightly at the end of each breath
to make it easier for the patient tc oxhalc
 pressure ramp option that starts pressure at low level and slowly increase over a
period
3. Technical Specifications:
3.1 Display:
 Should have 3" or more LCD/LED/TFT display.
 Display Parameters: Inspiratory and Expiratory pressure, Inspiratory and Expiratory
time,
 Fi02 [%] Mean Airway Pressure (MAP), Air leak [%J, Temperature (T) etc.
3.2 Modes: CPAP, Spontaneous/times (S/T), S (Spontaneous), T (Timed) etc.

3.3. Operation mode: Continuous, standard for hospital use.

3.4. Pressure setting:
 Pressure setting from 4 to 25 cm H2O or more, adjustable in 4 steps or more.
 IPAP: 4 to 25 cm H2O or more
 EPAP: 4 to 20 cm H2O or more
 CPAP: 4 to 20 cm I120 or more
 Breathe rate: 5-30bprn or more.
 Ramp duration: Automatic, 0 to 45 minutes or more
 Should deliver the intended pressure constantly and accurately Easy to clean/sterilize
3.5 Air Oxygen-Blender Fi02 cancentration slio utcl b adjustable (21-100%) and accurate
3.6. Humidifier:
 Should automatically regulate the required temperature
 Should be a closed system for filling up water
 Should display the chamber temperature and temperature at the patient end.
3.7 Patient circuits:
 Should have the option of using both disposable and reusable circuits
 Air hose length should be 6 ft.
3.8. Data Storage: Should have the data storage and data transfer facility.
3.9. Alarm:
 High/Low Temperature
 Breathing circuit disconnection
 Lack of water
 System failure
 Power failure
 Low battery etc.
3.10. Battery backup: Should have inbuilt battery back-up for at least 60 min.
3.11. Safety Features:Limiting the delivered pressure in the event of an occlusion etc.
3.12. Portability: Mounting tray and support stand with at least 2 castors fitted with breaks.
3.13. Power Supply: Power input to be 220-240 VAC, 50 Hz fitted with standard plug.
3.14. Accessories: All standard accessories of the offered item must be provided with the
following:
 Inlet bacteria filter, if applicable - 05 nos
  Expiratory filters high efficiency — 05 nos
 Nasal mask for adult, with tubing — 04 nos
 Nasal mask for pediatric, with tubing — 02 nos
 Oral mask for adult, with tubing — 04 nos
 Oral mask for pcdiairic, with tubing-- 02 nos

4. Quality Standards & Safety:

 The offered item should be US-FDA/EU-CE/ JIS) approved product (EU-CE
should be from notified body), certificate of the offered item must be submitted with
the offer
 Brand and model must be engraved/embossed/printed on the machine (sticker not
applicable)
 Offered Model should be Brand new, latest model/version and from current
Production not before 2020, a declaration certificate from the manufacturer must be
submitted with the offer. Discontinued product will not he acceptable.

5. Warranty, Spare Parts Availability & After Sale Service:

 Three (03) years comprehensive warranty with all spare parts and accessories
(without consumables) after the date of installation & commissioning (functioning).
 Availability of spares parts must be for 5 years after the date of
installation commissioning (functioning).
 The service should be provided by supplier/local agent and should have local
service facility. 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/maintenance manual. The repair /maintenance
work have to carry out within 24 hours after getting request from user.
6.Installation: Installation and commissioning (functioning) by trained engineer should be
completed at earliest and reports must be submitted to CMSD in prescribed format.

7.Documentation:
 Catalogue/data sheet must be submitted with the offer.
 List of the consumables, standard accessories & parts with the price of the offered
item must be submitted with the offer. ,
 One set user manual for each machine should be provided during supply of the
equipment (photocopy not accepted).