Centre available telephone facilities that

would be
provided`

SCHEDULE OF REQUIREMENTS
Bidder should have below
noted Minimum Average
Sl No Item Name Total Qty EMD AMOUNT
Rs
Annual Turnover in last
three years 2020-21, 2021-22
& 2022-23.
1 MODULAR OT 114 1,76,00,000.00 Rs 176 Crores

TECHNICAL SPECIFICATIONS FOR MODULAR OT-20x20

All products should be designed and manufactured according to ISO 9001:2000 standards. System of stainless
steel wall panel’s Stainless Steel 304 1.4301, powder coated, ceiling panels, interior doors and windows
should be designed for operating theatres, as well as rooms in which high sanitary and hygienic standards are
required.
1, Steel panels are easy to clean and disinfect, and bacteriostatic, which offer high grade of sterility, what
shortens time between operations
2. Steel panels should be quickly installable.
3. Easy installation under the panels
4. Quick dismountable and refixable panel and modernization of installation underneath
5. With additional strengthening elements it is possible to mount on panel surgical scrub sinks,
shelves, cabinets etc.
6. Steel panels guarantee high mechanical resistance

SUPPLY, INSTALLATION AND COMMISSIONING OF MODULAR

OPERATION THEATRE CONSIST OF FOLLOWING:

1. Wall Panels
2. Ceiling Panels
3. Laminar air flow Box
4. Peripheral Lighting (inside OT)
5. Automatic/Manual, Sliding/Swing Door as per site condition
6. Touch screen OT control Panel for climatic control
7. Anti static and Bacteriostatic Flooring
8. X ray view Box
9. Storage Cabinet
10. Magnetic Writing board
11. Surgical Scrub Sink
12. Operation Theatre Pendants (Surgeon and Anesthestist)
13. Operating light LED
14. Medical Gas Pipeline (inside OT) with integrated alarm system
15. AHU & Ducting OT specific
16. OT grade power with redundancy (UPS)
17. Air Curtain
18. OT Table (Optional)

1 – WALL PANELS

1. Stainless Steel Prefabricated Walls

• Wall panel elements are made up of powder-coated chromium-nickel stainless steel, material EN1.4301
with a thickness of 1.0 mm. It should be tested & certified as per DIN 4103 / DIN EN 18183 / PN-EN
 10088-1:2007 and PN-EN 10088-2:2007. The wall panels are reinforced with gypsum board 12,5mm
thick, compliant with the norm PN-EN 520:2004+A1:2009. The total distance between the inside and
outside surfaces of the operating room should be variable to suit the architect’s layout, but should be
sufficient for the flush mounting of equipment. The cavity between the inner and outer walls should
be left with minimum obstructions for the possible addition of equipment at a later date and to enable
services, pipes, conduits etc., to be run within the cavity. Wall panel color combination (dual color
paneling) shall be as per approved shade by the end user during approval of construction drawings.

• All wall-mounted equipment should be flush mounted. The wall panel design and construction should
allow for the installation and support of all equipment and the provision of openings required for
installations, without affecting rigidity and strength.

• There should not be any sharp edges and corners should be smoothened. A shell type substructure should
be designed as a non-load bearing wall. Main supporting profiles, made of galvanized steel profiles
2mm thick. The floor rails are mounted using clamp plates and screws with dowels into screed or
threaded rods with dowels into the unfinished floor. The individual wall panels should be made of
single Sheet with the width of as required on site maximum up to 1200mm. The individual wall panels
should be attached to each other with removable clamps or screws or an equivalent fastening system
which will allow fast installation as well as removal for service. Welding of wall panels on site will not
be permitted. The joints / Gaps between panels (approx..6 mm) should be filled with pushed-in
antibacterial silicone hermetic seal with silver ions additive, which must be added to seal in its
manufacturing process. Liquid silicone should not be used for sealing. Once fixed they have to provide
complete hygienic sealing. The prefabricated wall panels should be coated at the factory itself. It
should have high heat stability and it should be highly durable against mopping. The coating should be
done at the factory of origin of the panel and it should not be done at site. Shade of coating should be
confirmed with the user department. Resistance against recommended hospital cleaning and
disinfection agents must be ensured. Certification from regulatory authorities is essential.

1.1 Antibacterial coating: Wall panels should be made of stainless chrome–nickel steel EN 1.4301
powder coated in any RAL color with silver ions added to the coating during production process.
Nanotechnology should be used to guarantees 24-houres protection against bacteria, fungi and mold including
Methicillin resistant golden staph, Salmonella, Escherichia coli and Legionella. The above should be
confirmed with adequate certificate, license or license agreement.

1.2 Picture on wall panel: According to choice by the user the panel with graphic as per following
specifications should be provided.
• Wall panel should be powder coated with thickness of metal sheet min. 1 mm and it should be
manufactured in multilayer technology. From the front side, metal sheet should be bent at the right
angle backwards at the top and bottom of the panel. Sides of the panel should be Z-shape bent to
allow for invisible mounting of the panel to the substructure. From the back side galvanized steel
sheet should be used, DX51D+Z140 or higher, according to the norm EN 10346:2011 / PN-EN
10346:2011, reinforced with gypsum board 12,5mm thick, compliant with the norm EN
520:2004+A1:2009 / PN-EN 520:2004+A1:2009.
• Surface finishing of the wall panel should be tempered safety-glass pane 5mm thick, resistant to
disinfectant typically used in operating blocks, complying with the requirements of norm EN ISO
12543-2:2000/A1:2005 / PN-EN ISO 12543-2:2000/A1:2005. Decorative graphics or colored
plastic foil should be sandwiched between the glass and steel panel; alternatively paint coating
applied directly on the glass panel.
• -Panel construction must later allow for easy dismantling of a single panel to make additional
changes of installations inside the wall.
• Wall panels, safe glass faced, mounted on the substructure–supporting profiles made of galvanized
steel, should allow for installation of medical gases, electrical wires and sewage system inside the
walls if required.
• Gaps between panels (should not more than approx. 6 mm) should be filled with pushed-in
antibacterial silicone hermetic seal with silver ions additive, which should be added to seal in its
manufacturing process. Using nanotechnology guarantees 24-houres protection against bacteria,
fungi and mold including Methicillin resistant golden staph, Salmonella, Escherichia coli and
Legionella. The above should be confirmed with adequate certificate, license or license agreement.

1.2 Fire protection: The wall system (panels and substructure) should be made of non-flammable
material. No dangerous concentrations of gases should be produced in an event of fire. It should
confirm to Class A2 & should be in accordance with EI 1363-1, EI 1364-1 standards.
2.0 CEILING PANELS

Ceiling system for operating blocks consequently should supplement the modular wall system. Panels in
modular ceiling system should be 600 x 600 mm and should be adjusted to the distance between axes of
elements of ceiling substructure and can be dismantled separately.

Prefabricated elements which constitute the ceiling system.

a) Substructure - Lower substructure should consist of bonds connected by clamps, made of supporting
and cross profiles, which should form a stable construction. It should be regulated with the use of
mounting rods with nonius hanger at the height between 300mm and 1100mm. Rods with nonius
hanger should be attached to the real ceiling with metal dowels. The arrangement of suspension points
should correspond with the static requirements of ceiling construction and should take into account the
ceiling grid and conditions of infrastructure installation. All elements of substructure base should be
made of galvanized material. Ceiling panels should be suspended in the supporting profile with a clip-
in system. Ceiling system should guarantee even leveling of ceiling surface, as well as easy removal
and replacement of ceiling panels.

b) Ceiling panels made of stainless steel - Ceiling panels should be made of high quality stainless chrome–
nickel steel (0,6-0.8mm thick) EN 1.4301 optionally powder coated in any RAL color with silver ions
added to the coating during production process. Using nanotechnology guarantees 24-hours protection
against bacteria, fungi and mold including Methicillin resistant golden staph, Salmonella, Escherichia
coli and Legionella. The above should be confirmed with adequate certificate, license or license
agreement.

c) Standard panels dimensions should be 600x600mm.

D) Ceiling panels mounted in the substructure shall be individually removed.

3 LAMINAR Supply System

To guarantee supply of highly filtered air above operating zone by using laminar flow unit with three stage
filtration minimum of H14 level.

•• Laminar diffuser should be made of stainless steel 1.4301 or 1.4016, surface finishing – natural color
of stainless steel or color adjusted to the color of the ceiling.

•• Laminar diffuser should be supplied by the manufacturer of the modular wall and ceiling system,
which guarantees full compatibility of used solutions.

•• Laminar diffuser should have a certificate allowing it to be used in operating theaters.

•• Laminar diffuser must be selected in such a way that the supply clean air stream encompasses all
areas in the operating room requiring special protection (ie. the operating field, operating team,
instrument table – the size of a required laminar ceiling depends on the type of operation being
conducted.

•• Selected laminar diffuser should be characterized by non-turbulent flow of air (degree of turbulence
<5%), surface of diffuser should be made of stainless steel mesh which serves as the air flow
divider used to align and stabilize the outflowing stream of air.

•• The outflowing air from the laminar diffuser to the operating room must go through a highly
efficient final filter of at least class H14 (filter class according to EN 1822-1/ PN EN 1822-1).

• Size of laminar box should be designed by the modular operation theatre supplier according to the
requirement of air exchange, whole volume of the air in the operating theater, based on type of the
operating theater.

• Air volume flow should be designed individually for every single operating theater individually by
operating theater supplier.

• The laminar flow unit should not be riveted or screwed with sealed gaps.
• Frame of the laminar flow unit must be tightly welded from stainless steel SS 304 only.
 • The system shall be vibration free due to Air flow as per HVAC design
• The system shall have integrated Pressure relief valve system for Approrirate Positive pressure
management system inside the Operation theater
• Positive Pressure Monitoring system

Air exhaust ducts

• Air exhausts grids should be provided in corners of rooms and should be connected to the exhaust
channels placed behind wall panels.
• The exhaust channels should be connected to air exhaust grids at both locations, close to the floor as well
as close to the ceiling.
• Part of them must be provided with regulation valve and metal removable filter.
• Grids should be made from stainless steel.
• Metal filter is set on bottom exhaust grids.
• Bottom exhaust grids should be at 300 mm from the floor and upper exhaust grids at 300 mm from the
upper edge of the lower ceiling.

•• Upper exhaust grill should exhaust 30% to 40% volume & lower grill should exhaust
60% to 70% of volume.

4 PERIPHERAL LIGHTING SYSTEM

• Lighting in the operating theater must be in accordance with European standard / ANSI and international
standards.
• Minimum required IP protection is 54 and intensity of lighting in operating theater should be min. 1000
– 1500 lux.
• Light fittings should be installed into level with ceiling and will be covered by tempered glass and
optical grid.
• The color temperature of the light should be 5700 - 6500 K.
• Color of visible parts of lighting fitting must be in accordance with color of ceiling cassettes. The
intensity of lights should be controlled by electronic stabilizers.

5 DOORs

Manual Sliding/Swing Door

• Doors should be manufactured of the highest quality stainless steel.

• Stainless steel ( 304 grade) thickness 1 mm polished
• Doors construction should properly fit with wall panels and should create a uniform system of the
operating theater.
• Doors should be made as sandwich-type – from two plates, the space between them should be filled with
particle board or with so called honeycomb, glued to the plates. In installation places of hinges and
locks, strengthening components must be used.
• Thickness of door wings should range in between 40 and 60mm.
• Frames should be integrated into the panel system and should be prepared individually for each type of
door, made of stainless steel 1, 5 mm thick.
• Fixtures should be made of stainless steel and adapted to requirements – size and weight of door wings,
shape of door handles prevents form hooking the aprons.
• Main door should be sliding or swing manual as per site condition – automatization of the door should
be quoted as optional.
• If automatic door chosen, automatic equipment for door should be provided by reliable manufacturers.

• Operation of door should be realized through a wall board, elbow buttons or touch less buttons for
operating room only and normal doors for sterile room
• The door should be hermetically sealed.
• Operation of door should be realized through a wall board, elbow buttons or touch less buttons for
operating room only.
• Doors should be able to be equipped with door viewers, windows used for room observation.
6 MULTI FUNCTIONAL PANEL – TOUCH SCREEN TYPE – 21 inch

Touch screen Control panel must be able to show temperature, humidity in the operating theater and must be
able to be set on required temperature of air as well as light intensity. Also must show function of clock and
stopwatch. OT Room Parameter Monitoring should be 21 Inch LED Touchscreen. Test Certificate, Calibration
Certificate should be provided. Should be Stainless Steel Flush medical grade Mounted Easy-to-clean.

The panel should have below mentioned features

• Temperature Display with Hi, Low Alarm

• Date & Time Real Time Clock

• OT Room Differential Pressure with Hi, Low Alarm -Optional

• Temperature & Humidity & DP Control

• Dirty Filter Display and Alarm-HEPA-Laminar.

• Operating or Elapsed Time

• Anaesthesia Countdown

• Medical GAS Hi – Low Alarm System

• Humidity Display with Hi, Low Alarm

• Dimming Illumination of Operating Room

• UPS and Power Line Alarm -Optional

• Report of Environmental Values

7 FLOORING

• Flooring is required in minimum standard.

• Color shades should be in accordance with color shade for surroundings.
• Flooring should take up to 100 mm to the wall.
• The connection of wall with the floor should ensure easy cleaning.
• 2mm Thick Flexible Homogeneous vinyl Floor covering with an electrical resistance of 5 x 10 (4) ≤ R ≤
10(6) (EN 1081). The conductive carbon coated PVC pellets create the permanent static-conductive
properties. It complies with EN 649.
• The Flooring shall be as per the Medical standards

8 X RAY VIEW BOX - LED

Twin - X- Ray viewer with option of vertical as well as horizontal covering must be flushed into
operating theater wall. The dimming function should be provided.

9 STORAGE CABINETS
• Modular system of built-in operating theaters must enable possibility to install different types of
cabinets based on customer requirements, which must be flushed into place behind wall panels.
• Those cabinets will be installed in situation, where customer will require them and they will be part of
drawing documentation and price offer given to customer.
• Those cabinets must be in same color shade as wall panels and doors to achieve uniform look of
operating theater.
• The storage cabinets will be made of SS304 grade

10 MAGNETIC WRITING BOARD

One operating list board should be provided in each operating theatre .It should be made of Magnetic
glass properties and should be flushed to the wall of the operating room.
11 SURGICAL SRUB SINK

• DOUBLE tap Foot Operated & SENSOR OPERATED SURGICAL SCRUB

• WITH Integrated SOAP DISPENSER.
• SIZE – 1500 (L) X 565 (D) X 1365 (H) MM.
• SS 304 GRADE, SS 1.2 MM THICKNESS.

12 – PENDANTS

Should comply with the following standards and specifications:

• Ceiling supply unit shall complies to class II B of medical device directive, and also shall complies with
EN ISO 11197 which include Heavy duty ceiling assembly kit, mechanical safety, oxygen enrichment
test, electrical safety test and high quality flexible hoses. The device should be CE marked.
• The device shall meet the basic safety and essential performance as per IEC 60601-1.
• The device shall meet the electromagnetic disturbance - requirement and test as per IEC 60601-1-2.
• Risk assessment for the ceiling supply unit shall be verified as per DIN EN ISO 14971.
• Manufacture shall provide the device with the Symbols to be used with medical device labels, labelling
information as per ISO 15223-1
• The medical rail system of the device shall complies with DIN EN ISO 19054.
• The device shall meet the ingress protection class IP2x as per DIN EN 60529.
• The device shall have low pressure hose assemblies for the use with medical gases and must be durable
and shall meet medical grade criteria as per ISO 5359.
• The device shall have the terminal unit for medical gas pipe line that meets EN ISO 7190-1
• The device shall have down light for floor illumination.
• Pendant arm should be available in the length of 500 ,750 and 1000mm. The smooth and corner less
design of arm ensure smooth and easy cleaning.
• Arm must rotate 330˚ degree and should have friction break for easy gliding and also should be equip
with mechanical end stop
• Column Size should be in the range of 230mm x 275 mm and arm size should be 175 mm x 105 mm
with a max load capacity of 80 Kg.
• The pendant must have robust and modular construction, should be constructed from robust, extruded
aluminum profiles. Rounded corners, edges and seamless fittings ensure safety, hygiene and easy
cleaning.
• It should have a flexible positioning and the Rotation feature of the pendant column to gives the user the
flexibly to position the medical devices up to 330˚ about the vertical axis.
• Accessories like shelf should consists of powder coated aluminum which provide smooth, scratch
resistant quality. The corner of the shelf features rubber attachment to protect against collision for safer
use.
• High Quality medical rails compliance to the international medical standards are fitted on both side of
the shelf that allows user to add more devices on to it. shelf dimensions should have 480 x 400 mm,
The load capacity of shelf alone should be 40 kg and together with medical rails it goes up to 50 kg.
• Drawer can be optionally be added below the shelf. The smooth slides of the drawer ensure noiseless
operations
• The height adjustable infusion pole should be suitable for attachment of up to 4 bottle holder. The stylish
and ergonomic design provide scratch free surface.
• The 500 mm long Swivel arm and adjustable pole should allow user to position the bottle holder within
wide range of reach

A: Anesthesia Pendant – Single Arm –

Horizontal Arm: Double Arm - 1000 mm.

Load capacity for Arm – 80 Kg or more
Vertical Media Column: 1000 mm or more
Gas: 2 x O2, 1 x N2O, 2 x Vac, 1 x Air 4, 1 x AGSS Venturi System
Electrical Sockets - 12 nos
Braking system – Friction.
Accessories
• IV pole – 1 Nos
• Shelf with side rails - 1 Nos
 o Size – 430 mm x 480 mm with load bearing of 40 kg or more.
o Drawer - 1 nos

B: Surgeon Pendant – Single Arm –

Horizontal Arm: 1000 mm

Vertical Media Column - 1000mm or more
Gas: 1 x O2, 1 x Air 7, 1 x Vac, 1Air 4
Electrical - 8 nos
Braking system - Friction
Accessories
• Shelf with side rails - 3 Nos
o Size – 630 mm x 480 mm with load bearing of 40 kg or more
o Drawer - 1 Nos

13 - SURGICAL LIGHT DOUBLE DOME LED CEILING MOUNTED

• The double dome operating light must be designed for the use in high demanding surgical procedures.
State-of-the-art LED bulbs should be used to ensure a low energy consumption and a long service life.
• Revolving outer handles at the light head should be provided to allow for non-sterile positioning.
• Light head must be designed with smooth transitions and surfaces, without slots, gaps or exposed
screwing to ensure fast and effective cleaning.
• The light head with streamlined shape is favorable within laminar flow. The light head must be resistant
to disinfectant.
• For sterile positioning an ergonomic, exchangeable and centrally positioned sterile handle within the
light head should be provided. The sterile handle should have adjustment control for light intensity and
light field diameter for ease of control.
• All main joints of surgical light must be provided with unlimited rotation (360°). Light head and
suspension must be sealed dustproof.
• All domes should have Illumination intensity of endo light - 3,000 lux
• Bulbs should life of more than 50,000 hours.
• Classification
▪ Protection class acc. to IEC 60601-1 -
▪ Multipurpose switching power supply - Protection class 1
▪ Light body – SELV
▪ Arm system – IP41
▪ Light body – IP42
▪ Ventilation and air conditioning Part 4 - DIN 1946-4:2008-12
▪ Electrical installation - IEC60364-7-710/VDE0100-710
▪ Product design - IEC60601-2-41/IEC60601-1
▪ Electromagnetic compatibility (EMC) - IEC 60601-1-2
▪ Classification as per EC Directive 93/42/EEC EC/EE IX - Class I

• The surgical light should be complete with all components for ceiling mount and electrical feed-
in, incl. finalized installation.

(a) Technical data for main dome: - 1nos.

i. Central illumination intensity Ec 160000 lux

ii. Light field diameter at a distance of 1 m 200 mm

iii. Depth of illumination L1+L2 1300 mm

iv. Average Color rendering index Ra 95

v. Color rendering index R9 (red) 93

Color temperature 5000K
 vi. Central illumination at 1m distance with:

I. Tube 100%

II. one mask: 40%

III. tube and one mask: 40%

IV. two masks: 48%

V. tube and two masks: 48%

vii. Central irradiance Ee 580 W/ m² ± 50 W/ m²
viii. Ee/Ec ratio - 3.5 W/m2 x Lux
ix. Adjusting the illumination intensityF 40000 to 160000 Lux

x. Service life LED bulbs approx. 30000 hours

xi. Replacement of LED bulbs possible

xii. Ambient light mode (Endolight) 300 Lux

(b) Technical data for satellite dome - 1nos.

i. Central illumination intensity Ec 120000 lux

ii. Light field diameter 200mm

iii. Depth of illumination L1+L2 1300 mm

iv. Average Color rendering index Ra 95

v. Color rendering index R9 (red) 93

vi. Color temperature 5000K
vii. Central illumination at 1m distance with:

I. Tube 100%

II. one mask: 41%

III. tube and one mask: 41%

IV. two masks: 49%

V. tube and two masks: 49%

viii. Central irradiance Ee 430 W/m2 ± 50 W/m2

ix. Ee/Ec ratio 3.5 W/m2 x Lux

x. Adjusting the illumination intensity 40000 to 120000 Lux

xi. Replacement of LED bulbs possible

xii. Service life LED bulbs approx. 30000 hours

xiii. Ambient light mode (Endolight) 300 Lux

14 – MEDICAL GAS PIPELINE

All related copper pipelining inside the OT area is responsibility of the successful bidder. The copper pipes
will be as per EN 13348 standards approved from independent authority. It can be indigenous with required
certifications.
15.AHU (HVAC) Must be Rooftop type (RTU) and independent for each OT

AHU – AIR HANDLING UNIT (DOUBLE SKIN TYPE) Type

1. The air-handling units are of doubles skin construction, draw-throaty decompressing of various
sections such as Pre-filter section, coil section, and include din schedule of quantities.
2. Unit must be able to work satisfactory in exposed atmosphere conditions.

Casing
3. Double skinned panels are fabricated with an anodized extruded aluminium extrusion
frame work bolted together with sandwich panel having powder coated 0.70mm sheet for outer
skin and plain GP0.63mm sheet for inner skin.43mm thick PUF insulation material is injected
between the two panels (with U value no greater than 0.85 W / m2 / k)
4. The entire frame duly painted is mounted on sheet steel channel. The panels are sealed to the frame
work by heavy-duty 'O' ring gaskets held captive in the framed extrusion.
5. All panels are detachable or hinged. Hinges are made of die cast aluminium with stainless steel
pivots, handles are made of hard nylon and be operational from both inside & outside of the
unit.
6. All fixing and gaskets shall be concealed.

Motor and Drive

7. Fan motors are highly efficient and work on 440±10%volts, 50 cycles, three phases with explosion
proof type with class F installation, with IP55 protection.
8. Motors are especially designed for quiet operation and motor speed does not exceed 1440 rpm.
9. Drive to fan is provided through belt-drive arrangement.
10. Belts are of the oil-resistant type.
Fan
11. Fan are of centrifugal type, conforming to AMCA 210 and are double width, double in let with
forward- inclined airfoil blades, specially designed and suitable for the required operating pressure.
12. Fan casing are made from galvanized steel sheet.
13. Fan shaft is grounded C40 carbon steel and supported in self-aligning plumber block operating less
than 75%of first critical speed, grease lubricated bearings.

Cooling Coils
14. DX coils have 12.5 to15 mm diameter tubes minimum 24G thick with sine-wave aluminium fins
firmly bonded to copper tubes assemble din-zinc coated steel frame.
15. Face and surfaces areas are such as to ensure rated capacity from each unit and such that the air
velocity across the coil does not exceed 150 meters per minutes.
16. Each coil is factory test edat21-kg/m2 air pressures under water.
17. Tube is hydraulically / mechanically expanded for minimum thermal contact resistance with
fins. Fin spacing is 4 – 5 fins per cm.
Filter
18. Each unit is provided with a factory assembled filter section containing washable synthetic type
air filters having anodized aluminium frame.
19. The media is supported with HDP mesh.
20. Filter banks are easily accessible and designed for easy with drawl and renewal of filter cells.
21. Filter banks face velocities do not exceed 100m /minutes.
22. Differential pressures which is to be fixed across the filter as part of AHU's system.
23. Pre filters must be installed with the air duct to prevent heap filter to clogging
Ducting
24. The duct supply system should be free of construction debris.
25. Ducting shall be made of Aluminum (22 gage) with curves & bends where indicated for easy
flow of air and ensured to be air tight by applying silicon seal ant after fabrication.
26. Hangers shall be provided to ducts &shall be suspended by means of G.I. coated rods & these
shall not be more than 2.5mtrs apart.
27. Thermal insulation with 11mm -18 mm 9mm XPE for supply & return air ducts. Joints will be
lapped with Nitrile rubber tape for better insulation.
28. The designed must be such a way that, there must not be sweating inside the OR complex
throughout the year in any weather condition.
Air Cooled Package Chiller/ Condensing Units.
Compressor
29. The compressor shall be of screw / scroll type, hermitic, in accordance with ARI520, direct
driven with capacity control arrangement.
30. The compressor casing shall be of cast iron and designed for 450 psi goes or higher.
31. The compressor shall in corporate rolling element bearing to support rotating assembly.
32. The rotor shall be higher steel alloy.
33. Refrigerant circuit components shall include flexible pipe connectors, hot gas muffler, high side
pressures witch, liquid lines hut-off valves, suction and discharge shut-off valves, filter drier,
moisture indicating sight glass, electron icon thermostatic expansion valve (EXV), heavy duty
 pressure gauge with cocks to monitor suction, discharge and oil pressure and complete
operating charge of refrigerant and compressor oil.
Motor
34. Compressor motor shall be of Hermetic/ semi-hermetic direct drive, squirrel cage, two poles,
induction type, and refrigerant cooled motor suitable for 415V / 50Hz.3phase supply.
35. Hot gas motor cooling is not acceptable.
Condenser
36. Condenser shall be Air Cooled type.
37. Tubing shall be copper, Aluminium fins high efficiency type.
38. Tubes shall be nominal 19mm. Outer diameter and thickness shall not be less than 22g. and
rolled into rube sheets and shall be individually replaceable and also tubes shall be coated with
corrosion resistant coating.
39. Condenser fans shall be direct coupled to motor and protected against over loading and with
minimum
1.15 service factors.
40. Condenser shall design to allow isolating refrigerant charge when servicing the compressor.
41. The designed must be such a way that, there must not be sweating inside the OR complex
throughout the year in any weather condition.
42. System offered should comply with the above technical specifications, the Air Handling Unit
with Air Cooled Package Chillers / Condensing Units should have adequate capacity as per the
airflow/air pressures and air changes calculated as per different OTs & other utility area should
maintain a temperature range between 18 -24 Degree Celsius
AC DUCTING
43. Ducting should be made of Aluminum (22 gage) (INSIDE OT ONLY), with curves & bends
where indicated for easy flow of air and ensured to be air tight by applying silicon sealant
after fabrication.
44. Hangers should be provided to ducts & should be suspended by means of G.I. coated rods.
45. Thermal insulation with fiber glass & with aluminium foil for supply & return air ducts.
46. Joints will be lapped with Nitrile rubber tape for better insulation.
47. The ducts should be connected to HVAC system provided by the Institution Outlets and Inlets
would be brought up to the OT area from where the same is to be connected to the Laminar flow
and return air system as well as to the common area and rooms in the OR COMPLEX
AIR DUCTS FOR RETURN AIR IN OPERATING ROOMS & CORRIDOR (AC
OPERATIONIZATION)
48. Exhaust air cabinet installed in corner.
49. Made of Aluminum / Galvanized Steel, standard channel cross section appr. 625 x 425 mm.
50. Exhaust channel as cabinet with upper & lower inlet, for room height 3000 mm. Incl. wall
cut-outs, revision door, sealing frame, traverses & fixation elements.
Cascade Pressure Stabilizer

51. Cascade pressure stabilizers should be multi-bladed units specifically designed to control
room air pressures in critical areas, such as operating theatre suites.
52. Each stabilizer should comprise of carbon steel housing with Grade 304 Stainless steel blades,
which pivot upon sealed for life bearing assemblies.
53. Balancing is carried out utilizing a proven balance weight assembly. These stabilizers should be
accurate to arrange of 1 Pascal over their working range of 5 – 35 Pa.

16. Uninterpreted power supply (UPS)

TECHNOLOGY Should be digitally controlled, IGBT based double

conversion On-line VFI according to IEC62040-3
specification, Inverter and Rectifier both should
1 be IGBT based
Built-in Galvanic Isolation Transformer (Delta to Star
connected) should be provided on the Inverter output
(External IT will not be accepted). Output
Neutral with Ground voltage should be <1 V
Input : 10KVA

2
Rated voltage 400 VAC three-phase + N
Voltage Range -25% +20% at full load
Frequency Range 45 to 60 Hz
 THDi <5%
Power Factor > 0.95
By Pass (Static & Manual both)

3
Rated Voltage 230 VAC single-phase
Permitted voltage ± 15% (should be selectable from ± 10% to ± 20%
range from front panel)
Rated Frequency 50 Hz
Permitted Frequency ± 2% (should be selectable from ± 1% to ± 5%
Range from front panel)
Batteries

4
Type 12V Sealed Maintenance Free Lead Acid
Backup Time 15 Mins. at full load condition
Minimum VAH 28,800 VAH
Battery Make Amaron /Quanta / Exide Power Safe
Recharge Time 4-6 Hrs.
Output

5
Rated Voltage 230 VAC, Single-phase
Voltage regulation Not more than +/- 1%
Power Factor 0.9 or above
VTHD < 2% for Linear & <3% for Non-Linear load
Crest factor 3:1
(Ipeak/Irms)
Waveform Sinewave
Frequency 50 Hz
Frequency stability ± 2% (should be configurable via the control panel
with the Inverter in ±1-5%)
Synchronisation with
the bypass
supply
Frequency stability ± 0.05%
with the Inverter out
of Synchronization
with the bypass
supply
Overload 110% for 1 Hr., 125% for 10 mins., 150% for 1
min.
Efficiency Should be > 92% at full load
Protection

6
Back feed protection The back feed protection should be installed in
series with bypass SCRs.
Normal Protection Input, output, rectifier input, battery fuse, bypass
required fuse, short circuit etc. Thermal on system,
rectifier, bypass and inverter. Protection against
prolonged battery discharge
Environmental Conditions

7
Operating temp. for 0 – 40º C
UPS
Relative humidity <95% non condensing
Noise <65dBA at 1 m
Mechanical Data
8
 Protection Degree IP 20
of the cabinet
Cable input Must be Bottom entry
Display & Software

9
Minimum list of the • Rating of the UPS,
information should be • Input Phase voltage, line voltage and input
appear on the LCD frequency,
Display & LED • Output voltage, load percentage, apparent
Lights Provisions
power, active power and output frequency.
• Battery voltage, charge or discharge current,
working mode & internal Temp.
• Turn ON and OFF UPS, delete fault record
• Output voltage and frequency setup, battery
setup, change password setup, recovery to
default setup, LCD Displays time setup, UPS
auto start setup, UPS auto shutdown setup,
Buzzer setup, language setup.

• there should be provision for LED Light

indicators e.g. Fault indicator, Bypass
Indicator, inverter indicator, battery
indicator, input power indicator etc.
Communication & RS232 & RS485 interface communication port
Software
Advanced, Multi-platform Communication, for all
standard operating systems and network environments;
shutdown & monitoring software

There should be provision to install SNMP

hardware in future for remote diagnostics
Other mandatory features:

10
Reliability The total system (Charger & Inverter section) should be
controlled by redundant microprocessor system. If a
fault occurred to either of the microprocessors, the
power supply to the protected
load should not be interrupted
UPS must not be based on a single Power PCB with
Inverter, Charger or Rectifier on the same PCB. (so that
in case any one of these fails then the entire UPS
system becomes non functional and repeated failures
does not render the PCB un- repairable). Undertaking
stating that neither Charger, Rectifier or Inverter
sections will be located on a single PCB must be
provided by the
bidder.
 ECO Mode When the load does not require highest level of
Function protection, the UPS shall be able to work in an energy
saving mode. This mode shall be fully
programmable to adapt it to the load and customer
needs.
Mimic Display Mimic diagram should be provided to know the
status of the rectifier, inverter, battery and output.
Self Diagnostics The system should provide “EVENT RECORDING”
facility. The system can be able to store last 20 events
i.e. input voltage variation or out of tolerance, operating
conditions of the system at any time, it should include
cause of the fault and should be able to display the
name of the faulty area in terms of rectifier fault,
inverter fault, battery contactor fault etc. through code.
All events should be readable from front panel
LCD/LED of the system and also from PC/Laptop
through the RS 232 communication interface port.
Input Phase In the event of any phase reversal in the input
Reversal power source, the system should neither trip nor go to
battery discharge mode. It should works on
mains but with fault alarm indicating input phase
reversal.
Dual Input Support The UPS should support dual input, that means the
mains input and bypass input can be separated
power supplies
Auto restart facility The UPS should configure to automatically restart after
a mains supply failure or after the batteries
have become fully discharged
EPO (Emergency In the event of an emergency the UPS should be
Power Off) completely shutdown by pressing single bottom /
command
International Standards & Certifications:

11
Safety & EMC Should comply EN62040-1 & EN62040-2
Standards (Copy must be attached)
Certification The company should have ISO 9001:2008; ISO
14001:2004; ISO 50001:2011 &
OHSAS
18001:2007 certification
(Copy must be attached)
Accessories All accessories like wire, switches etc which are
12 required for the installation of UPS are to be provided
by the vendor.
17. Air curtain system

DIMENSION
LENGTH - 1218 MM
WIDTH - 230 MM
HEGHT - 212 MM
EFFECTIVE HEGHT - 13 FEET SPCIFICATON
NUMBER OF MOTOR - 01 NUMBER OF
BLOWER - 02
PHASE - SINGLE
BLOWER TYPE - ALUMINIUM
NOISE LEVEL - 50-70
POWER (HP) - 0.56 HP
VOLTAGE - 220V/50HZ
MOTOR POWER - 400 WATT
RPM (MAX/MIN) - 2700
CFM - 1100