List of Approved Makes For Civil Works
List of Approved Makes For Civil Works
List of Approved Makes For Civil Works
Unless otherwise specified, the brand / make of the material as specified in the particular specifications and in the list
of acceptable make attached in the tender, shall be used in the work.
In case of any difficulty regarding availability of, procurement or otherwise of approved brands specified in the
contract, the contractor can be allowed to use alternate equivalent brand of the material subject to written approval of
the UPPWD.
Sample of all the materials will be used only after approval of the UPPWD.
2 Solar Hot Water System HoneyWell / Solahart / Sol. Power/ TATA Power
Solar/Bosch/Solimpeks
3 Butterfly Valve Audco/Danfoss/Honeywell/Zoloto
4 Check Valve – Dual Plate Advance/Honeywell/Audco/Zoloto
5 Check Valve – Wafer Type Advance/Danfoss/Zoloto/Honeywell
6 CPVC pipes Supreme/Ashirwad/Astral
7 GI Pipes Tata Steel/Jindal (Hissar)/ SAIL
8 GM / Forged Brass Ball Valves Danfoss/Honeywell/Zoloto
9 Heat Exchanger GEA Eco flex/Alfa Level or equivalent
10 Hot Water Re circulation OR other DP – Holland/Grundfos /Xylem -ITT/ Wilo – Mather Platt
Pumps
11 Insulation for Hot Water Pipes Armacell – Armaflex/Eurobatex – Union Foam K-Flex/ Thermaflex
12 Level Controller & Indicator (Water) Auto Pump/Cirrus Engineering/Technika /Techtrol
13 Pipe clamp & supports Chilly/ Euroclamp/ Kanwal
14 Sluice Valves IVC/ Kirloskar/ Advance
15 Solenoid Valve Danfoss/ Avcon/ Honey well
Note:
1. The contractor will use one of the approved makes as approved by the Engineer-in-charge.
2. In case of different quality/pattern of same make, the pattern/quality shall be approved Engineer – in –
charge.
3. For materials/equipment/ to be used in items of work for which approved makes are not given here in,
the makes of such materials/equipment shall be as decided by Engineer–in- charge.
4. If any major equipment is using a small component of make other than that given as a standard
component with the equipment, the same shall be accepted subject to approval of Engineer–in-charge.
Approved Make - MGPS System
Sl.
Description /items Approved makes
No.
LMO Tank (20KL Primary Supply and 10KL Linde / Prax Air / Inox
1
Backup Supply)
Secondary Oxygen Manifold and Emergency
2 oxygen manifold with automatic control Atlas Copco / Amico / Ohio Medical /
panels Pneumatic berlin/Med Freshe
3 Atlas Copco / Amico / Ohio Medical /
Oxygen Flow meter with Humidifier Bottle
Pneumatic berlin/Med Freshe
4 Nitrous Oxide Manifold and Emergency NO2 Atlas Copco / Amico / Ohio Medical /
Manifold with automatic control panel Pneumatic berlin/Med Freshe/Reanimed
5 Co2 Manifold and Emergency Co2 Manifold Atlas Copco / Amico / Ohio Medical /
with automatic control panel Pneumatic berlin
Medical Air Supply System (4 Bar & 7 Bar) Powerex/ Atlas Copco / Amico / Ohio
6
complete. Medical /Pneumatic berlin
7 Medical Vacuum (suction) Supply System Powerex/ Atlas Copco / Amico / Ohio
Complete. Medical /Pneumatic berlin/Anest Iwata
Atlas Copco / Amico / Ohio Medical /
8 Vacuum Units (Ward/Theaters/Lowflow)
Pneumatic berlin
9 Powerex/ Atlas Copco / Amico / Ohio
AGSS system Complete
Medical /Pneumatic berlin
10 Copper Pipe : Mehta Tube(Maxflow) / Rajco
Distribution Piping Complete with
/ Metal Alloys (Metalco)
Accessories.
Fittings : Conex Banninger
Atlas Copco / Amico / Ohio Medical /
11 Gas Outlets with Probes
pneumatic berlin
Area Valve Service System & Line Isolation Atlas Copco / Amico / Ohio Medical /
12
Valve Pneumatic berlin
13 Atlas Copco / Amico / Ohio Medical /
Alarm Systems (Master & Area)
Pneumatic berlin
14 MPS/ PES/ Prenit/ MDD/ Active/ Eubiq /
Bed Head Panels (Vertical & Horizontal)
Medirail Systems/Med Freshe
15 High pressure tubes for O2, N2O, CO2, AGSS, Atlas Copco / Amico / Ohio Medical /
Compressed Air & Vacuum, Etc. Pneumatic berlin /Aktive
Everest Kanto / Rama Cylinders / BPCL (BIS
16 Gas Cylinders
Approved Only)
Note:
1. The contractor will use one of the approved makes as approved by the Engineer -in-
charge.
2. In case of different quality / pattern of same make, the pattern/ quality shall be
approved Engineer - in - charge.
• The pre-fabricated Operating Room should be Cladding structure insulated Stainless steel wall
panels. Total Panel thickness 50-60mm.
• The SS Sheet of minimum 0.8mm thick made up of 304 Grade Stainless Steel. Sandwich
panel (Both side0.8mm SS 304 Sheet) with core consisting of rigid polyurethane foam,
which has been injected under high pressure, with a minimum density of 40 kg/m3.
• The individual wall panels shall use the tongue and groove technology for joining two panels,
no welding should be allowed. The tongue & groove should be of steel and easy to operate.
• The gaps between panels shall be suitably filled with metal filler/epoxy and sanded flush.
• Stainless Steel plate finished to fine grain surface, treated properly to take anti-fungal paint.
• Paneling should be easy to maintain, durable, antistatic/conductive and fire retardant.
• Clearance between inner panel and outer wall should be sufficient to allow the maintenance
personnel for service. This closed space should be flushed continuously to eliminate dust and
bacterial accumulation.
• Anti-bacterial paint should be coated on the wall.
• Bidder should maintain anti-bacterial paint during warranty and CMC period.
• Wall elements should be resistant to all standard cleaning agents, disinfectants and fumigation
agents.
• Panel should be covered with protective sheath to prevent scratch during installation.
• It should have minimum number of junction. The junction should be seamless and should be
sealed with suitable sealants.
• The wall panels should be CE/UL Listed/BIS/DIN 1.4301 certified
• Third party test certificate for SS304 from material testing lab(Govt. Authorized)-to be
provided at the time of pre dispatch inspection/supply.
• The pre-fabricated ceiling plates/cassettes should be made up of SS304 panels with sheet
thickness of atleast 0.6mm. Sandwich panel (Both side0.6mm SS304 Sheet) of PUF with
minimum density 40kg/m3 with matt finish and should be coated with anti-bacterial paint. It
should be from the same manufacturer of wall panel. Total thickness should be 30-40mm.
• Support elements: high quality Suspension bracket with tension spring.
• Material: High quality galvanized or powder coated steel.
• Room lighting, air supply inlet, ceiling service units, return air outlets, etc. should be integrated
with SS metal ceiling system.
• The individual panels except those at the edges should be removable individually.
• The ceiling material should be CE/ UL/BIS /DIN 1.4301 certified
• Anti-bacterial paint should be coated on the ceiling.
• Third party test certificate for SS304 from material testing lab.(Govt. authorized)- to be provided
at the time of pre dispatch inspection/supply.
• The ceiling filtration system should be designed to ensure unidirectional distribution of sterile
air of the surgical theatre to ensure the cleanliness of all the area covered by the air flow.
• The Laminar flow system should comprise of thick extruded aluminum profiles frame and
sealed gasket. The filters installed in the plenum should be suitable for application for laminar
flow and clean rooms. These filters should meet following specification.
Separators : continuous thermo plastic chord
Sealant :Polyurethane
Gasket : One piece polyurethane
MPPS average efficiency: > 99.95%
3 Micron DOP efficiency > 99.99%
Final Pressure drop : 600pa(max)
Maximum Operating Temp : 60 degree Celsius
Maximum RH : 40-50 %
• The ceiling system should be equipped with―H14‖ class HEPA filters position in the ceiling
to achieve 0.25m/sec flow at the diffuser.
• Filtration Ceiling System holding structure, Filter frames and top plenum should be made of
Aluminum/Stainless Steel.
• The filtration ceiling system should have diffuser/flow equalizer to achieve uniform &
constant air distribution over the whole surface. It should be CE/UL certified
• The air management system should be designed to achieve class 100 with the following
parameters:
Bacteriological class =B (5 CFU/m3)
Particle decontamination kinetics CP =5 min
ISO 14644/1 classification = ISO 5
• Third party validation by Govt. approved environment lab( After Installation)
• The positive pressure should be maintained inside the OT to prevent contamination due to air
from outside the OT.
• The supplier should provide test certificate for HEPA filter and laminar air flow systems
from the original manufactures.
• Size of laminar airflow system minimum 8 feet X 8 feet or more.
• Should be CE certified.
Note: Prospective bidders are advised to collect the information regarding CFM and AHU capacity from
the respective institute site. Total flow rate of filter bank shall match the CFM of AHU.
• HVAC Ducting & Exhaust System
• All the ducting inside the MOT shall be scope of the MOT bidder.
• All the ducting should be as per industry standard and sheet should be Aluminum of appropriate
thickness and insulated as per industry standard.
• All necessary HVAC interconnection for supply and return air shall be the scope of bidder (the
institute will provide the duct upto outside of each MOT)
• Return air exhaust grill should be provided in the OT.
• The exhaust air cabinets should be openable and cleanable.
• These cabinets should have suction from bottom and top also.
• Designed flow rate should not be less than 1000 m3/hr. Distribution of exhaust air volume
should be divided between fluff strainers to maintain the required pressure within the theatre
without causing turbulence.
• The Exhaust air cabinet should be manufactured and supplied by the supplier of wall and
ceiling system supplies.
• Return air exhaust cabinet should be made from SS304 and should be from the same
manufacturer of wall panel. Also it should match perfectly with the ceiling system
aesthetically.
• Door sizes should be as per below option and quantities will be as per BOQ of respective
institute
➢ HERMETICALLY SEALED DOORS Size 2.1mx1.8m
➢ HERMETICALLY SEALED DOORS Size 2.1mx1.0m
➢ HERMETICALLY SEALED DOORS Size 2.1mx1.8m with Lead Line(As per AERB
Norms)
➢ HERMETICALLY SEALED DOORS Size 2.1mx1.0 m with Lead Line(As per AERB
Norms)
• This should be a hermetically sealed, single sliding door of 2.1 (H)X 1.8 m(W)
• The controller should be capable of being operated by elbow switches/foot switches as well as
touch less sensor.
• The track should be of stainless steel/Aluminum and the running surface for the top rollers
should be suitably angled to reduce resistance to movement.
• The door leaf should be hung by means of hard plastic rollers of high quality with double
bearing at the top. Rollers should be provided under the stainless steel/Aluminum track to
enable smooth and noiseless movement.
• Opening and closing of the door should be microprocessor controlled electromechanical
movement.
• The door material should be of HPL Color should match the interior and care should be taken
to make the leaf strong and light weight.
• One should be able to open and close the door effortlessly in case of failure of automatic
mechanism.
• Door opening handle should be strong and sturdy. Material should be of SS (gloss finish).
Should be provided with high quality cylindrical lock.
• Door leaf should have high quality synthetic rubber gasket with long life to ensure hermetic
sealing (to maintain air pressure differential). Air tightness 99.99% at a pressure of 100Pa.
• The finished floor on either side of the door should be perfectly level (maximum permissible
difference +1mm).
• The overall thickness of the finished door should be 40-60mm. The inner part of the door
should be filled with CFC free polyurethane foam thickness of 48mm or nearby. (Sealed
airtight to prevent further ingress of any microbial organism).
• The door and controls should comply with IEE regulation. All motors used should be DC
brushless motor with essential isolation from mains.
• Door should be with vision window 300 mm x 300 mm with double glazed panels and
hermetically sealed.
• Door movement should have minimum noise.
• Thestartingtimeafterreceivingthesignalshouldbeadjustablebetween0.5to20seconds.
• The door controller should be CE marked.
• Test certificate for hermetically sealed door frame (factory test certificate) should be enclosed
with the pre dispatch documents.
• Hermetically Sealed Window with Motorized Blinds for MOT as per requirement. The approx.
1.5m x 1m or 1.5 x 1.5 m
• The OT control panel should be touch screen panel. This control panel should work as the
central control panel for the HVAC controls, instruction board. Touch screen, OT light control.
The controller should be capable of adjusting the temp adjustment of +/- 5 Deg with in
5Minutes. It should be CE or UL Listed.
• The touch screen should be wall mounted, stationed in the visibility line of the surgeon and OT
staff.
• The access height should be convenient for the nurse to operate and help/assistant when in
need.
• The panel should accommodate digital clock and the elapsed time indicator.
• The medical gas alarm should indicate high and low gas pressures for each gas service present
in the OT including vacuum. This should be supported by audible alarm also. The panel should
have an alarm mute (fault annunciation) facility. The sensors (pressure switches) should be at
the nearest isolation valve.
• Control for general lighting: ON/OFF and dimming controls organized in groups to provide
uniform illumination.
• Control of the operating light (major and satellite and camera control (on/off and intensity
control) should be provided.
• Hand free telephone set with memory should be located at one side.
• Temperature and humidity control for the room connected to the AHU. (Adjustable from the
panel) The controller should be capable of adjusting the temp adjustment of +/-5 Deg within 5
Minutes wherever separate AHU is provided for each OT.
• Digital room pressure indicator in cm of H2O or equivalent (signal from pressure sensor shall
be provided to indicate pressure differential between OT and outside)
• HEPA filter bank differential pressure indicator.
• The control Panel should be able to integrated with HIS/BMS
• The Control Panel should able to display the Isolation Panel Alarm Conditions along with
MGPS Alarms.
• The touch screen size should be minimum 32 inch color LED
• Pressure relief dampers or over flow ports should be provided in each room to prevent
contamination of air from clean and dirty areas.
• Suitably sized air pressure relief damper should be strategically placed, enabling differential
room pressure to be maintained and ensure that when doors are opened between clean and dirty
areas.
• Counter- weight balancing system should be provided in the PRD to maintain positive pressure
inside the operation room.
• Air pressure stabilizers should have unique capability of controlling differential pressure to
close tolerance. The PRD should remain closed at pressure below the set pressure and should
open fully at a pressure only fractionally above the threshold pressure.
• The frame, body and blade should be of grade SS304 stainless steel.
• It should be provided in each operation theater to remove waste materials from the operation
theater to dirty linen area/corridor just adjacent to Operation Theater.
• Each hatch box should be equipped with two doors and the door should be operated
electrically/motorized.
• The hatch should be designed in such away that only one door should be opened at one time.
• The UV light should be so installed that it is kept on while both the doors are closed. This UV
light has to be automatically turned off in case of opening of either of the doors.
• Indicators should be provided on both sides of the OT so that door open / close status can be
monitored from both sides.
• Hatch Box material should be SS304 grade.
• Size of the Hatch box minimum: 600mm x 600mm.
• Compact surgical scrub sink should be designed for use in OT complex providing for pre
procedural scrub up.(Double sink combination(2bay type) as suitable)
• Each fixture should be fabricated from heavy gauge type 304 stainless steel (minimum
thickness 1.5mm) and should be seamless welded construction, polished to a satin finish.
• The scrub sink should be provided with a front access panel which should be easily removed
for access to the water controlled valve, waste connections, stoppers and strainers.
• Hands free operation should include infra-red sensors with programmable adjustment.
• Thermostatic mixing, valve control should be located behind the access panel and maintain
constant water temperature.
• Timing should be adjustable to meet individual application requirements.
• Provided with infrared sensors, thermostatic control taps with fail safe temperature controls.
• All units should have reduced anti- splash fronts.
• Knee/foot operated switch should be provided additionally.
• The storage unit should be made with 1 mm thick stainless steel panels.
• The shelves should be of SS 304 & removable for cleaning.
• The storage unit should be divided 2 or more parts and each part should have individual glass
doors/or common glass door with high quality locking system
• Double arm moveable Pendant for Anesthetist. The Pendants should comply with NFPA
99C/HTM 02-01/DIN. The support arms should be extremely robust and revolve on high
quality bearings, so that the pendant head glides smoothly and quickly to any desired position.
• Double moveable arms (any combination) with total coverage of min 1800mm and 330 deg.
Horizontal movements for each arm. Vertical movement should be motorized and the arm
height should remain to a height greater than 6.5 feet above floor level.
• Weight carrying capacity of the arm should not be less than 180 Kg. should have
electromagnetic/pneumatic brakes.
• Each arm should be capable of 300-340 degrees of rotation, which can be easily adjusted to
suit the desired mode of operation.
• The pendant should be European CE Certified with 4digit notified body number or US FDA
approved.
• The Pendant Service Heads should be modular with minimum 1000mm head. The heads should
be capable of accepting a range of shelves, infusion poles, electrical switch/sockets, gas outlets
other accessories as asked in tender. The Pendant Heads should support the range of
• Physiological Monitor Mounting Solutions.
• The Pendant Service Heads should be supplied with medical gas terminal units and 5/15 or
6/16 Amps hybrid Sockets with switches.
• Double arm pendant anesthesiologist and surgeon : Each pendant should be supplied with
minimum outlets and probes as mentioned below –
➢ Oxygen Outlets – 2 nos.,
➢ Vacuum Outlets – 2 nos.,
➢ Nitrous oxide – 2 nos.,
➢ Air(4 bar) Outlets - 2 nos.,
➢ AGSS outlet - 1 no
➢ Electrical sockets - 10 nos.
➢ Adjustable Shelf with two rails one on each side – 3 no.
➢ IV Fluid Pole with 4 hooks – 1No.
➢ Data socket RJ-45 -2 nos.
• Pendant supplier should provide cutouts for Patch Panels in Integrated OTs. (only for
integrated OT)
• Double arm moveable Pendant for Surgeon
• The Pendants should comply with NFPA 99C/HTM 02-01. The support arms should be
extremely robust and revolve on high quality bearings, so that the pendant head glides
smoothly and quickly to any desired position.
• Double moveable arms (any combination) with total coverage of min 1800mm and 330 deg.
Horizontal movements for each arm. Vertical movement should be motorized and the arm
height should remain to a height greater than 6.5 feet above floor level.
• Weight carrying capacity of the arm should not be less than 180 Kg. should have
electromagnetic/pneumatic brakes.
• Each arm should be capable of 300 - 340 degrees of rotation, which can be easily adjusted to
suit the desired mode of operation.
• The pendant should be European CE Certified with 4digit notified body number or US FDA
under Medical Devices Directive.
• The Pendant Service Heads should be modular with minimum 1000mm head. The heads should
be capable of accepting a range of shelves, infusion poles, electrical switch/sockets, gas outlets
other accessories as asked in tender. The Pendant Heads should support the range of
Physiological Monitor Mounting Solutions.
• The Pendant Service Heads should be supplied with medical gas terminal units and 5/15 or
6/16 Amps hybrid Sockets with switches.
• Each pendant should have – Each pendant should be supplied with outlets and probes as
mentioned below –
➢ Oxygen Outlets – 1 nos.,
➢ Vacuum Outlets – 2nos,
➢ Air(7bar) Outlet- 01nos,
➢ CO2 Outlet - 01 nos.,
➢ Nitrous oxide – 1 nos.,
➢ Air(4 bar) Outlets - 1 nos.,
➢ Electrical sockets - 10 nos.
➢ Adjustable Shelf with two rails one on each side – 3 no.
➢ Data socket RJ-45 -2 no.
➢ IV Fluid Pole with 2 hooks–1No. (Pole should be capable of stacking 4 nos of syringe
pumps)
➢ Pendant supplier should provide cutouts for Patch Panels in Integrated OTs (only for
integrated OTs).
• To provide peripheral lighting and clean room luminaries with intensity min 500 Lux, it should
be minimum 8 in numbers for each OT. Should be with highly specular anodized aluminum
reflectors and optical antiglare system.
• Luminaries cover should be made of highly resistant, disinfectant proof laminated safety
glass/acrylic with stylish fine grained surface.
• The reflectors should be of high quality, cleanable and non-deteriorating.
• The white luminaries body should be made of sheet steel/ perfectly powder coated, supplied
ready for connection optionally for individual or series circuit with digital electronic control
gear in multiamp technology.
• Recess frames should be gas tight. The fitting should be flush with the ceiling and should be
removable from top or bottom. The light fitting should be uniformly and aesthetically
distributed on the ceiling to provide uniform illumination in the OT. Light should not interfere
when green mode endoscopy is performed
• Peripheral lighting should be done according to IP65 (international protection rating 65)/IP54
regulations.
• Control equipment for the general lighting and the light dimming should be provided in the
theatre control panel.
SCOPE: Electrical Installation
• Power distribution within the OT should be provided from distribution boards located local to
each theatre. Sub mains power to these panels should be by the general electrical contractor.
From these panels all distribution services within the departments should be run. Isolated power
supply, insulation measuring and protection as per IEC standards should be provided. This unit
should be EN/CE/UL/FDA/IEC certified.
• Earthed equipment bonding of all exposed metalwork should be provided.
• Power sockets within the Operating Theatres ancillary areas should be matched to the rest of the
hospital.
• Each wall of MOT should have minimum 02 Nos. 6/16A hybrid switch socket & 32A industrial
socket (For C Arm/Microscopes/Etc.) at any two walls as per IEC standard.
• Light fittings within the clinical areas should be recessed LED type with control gear
• Fittings should be sealed In accordance with the standard IP54.
• All equipment should be fully and permanently labeled to identify and describe the function,
operation and voltage of the apparatus concerned. Throughout and upon completion of the
electrical installation, tests in accordance with relevant sections of the local wiring regulations
should be carried out and the results recorded.
• All the conducting should be of MS/SS only as per IEC standard and suitable for hospital use
only.
• Isolation Panel System of minimum 10/20 KVA capacity (As per power requirement of MOT-
in case of 10KVA, bidder shall provide 2 nos. for each MOT to meet the power requirement)
should be provided for every operation theatre which ensures the safety of staff and patient.
System should have isolators provided through leakage relays etc. (If required) according to
IEC recommendation.
• This unit should be EN/CE/UL/BIS/FDA/IEC certified. These systems are to be commissioned
by specialists.
• Should be medical grade Insolation panel.
• Should have fault detection feature.
• Should be compliant to CEI 64-8 / IEC 60364-7-710/BS7671 Standard.
• Should be mountable on wall & compact.
• The IPS should be able to integrate with HIS/BMS and Surgeon Control Panel as standard.
• The bidder should ensure that all works carried out are to the recommendation made in the
• Department of Health and Social Securities HTM 02-01 /NFPA 99C / DIN
• Bidder should provide Oxygen, Air (4Bar & 7bar), Vacuum, AGSS, CO2 and Nitrous Oxide
supply to Operation Theatres from the existing lines terminated outside the OT .
• Bidder shall be responsible for supply, installation, testing and commissioning of complete
MGPS system inside the operation theatre including Distribution piping, Pendants, outlets and
other essential accessories.
• Terminal units should be gas specific and only accept the correct Medical gas probe. Gas
specific components shall be pin indexed to ensure that a correct gas specific assembly is
accepted.
• Each terminal unit should be identified by the appropriate recognized name or symbol, colour,
coding and shape as per HTM 02-01 /NFPA 99C. Outlets should be CE certified/UL listed.
• Copper pipes should be of solid drawn, seamless, deoxidized, non-arsenical, half hard,
tempered and degreased copper pipe. All copper pipes should be degreased & delivered capped
at both ends.
• The pipes should be accompanied with manufacturers test certificate for the physical properties
& chemical composition. The copper pipe should comply with EN 13348
• Copper pipe must have reputed third party inspection certificate (Eg. Lloyd‘s, TUV, SGS).
• Fittings should be made of copper and suitable for a working Pressure of up to 17bar and
especially made for brazed socket type connections.
• The copper fitting should comply with EN 1254-1
• The Brazing filler material should comply with EN 1044.
OT Light – LED
• Operating Room Surgical Lighting System should provide an ideal combination of
brightness, maneuverability, and shadow resolution without sacrificing color accuracy
through a consistent LED technology.
• Such Lighting System should have the following technical specifications:
➢ Number of Light heads : Two per suspension
➢ Color Temperature range: 3800k-5000 (±10 %)- Variable color temperature.
➢ Field Size Diameter : 20 to 28cm (+/- 10%)
➢ Working Range : 750 to 1100mm (+/- 10%)
➢ Illumination Level : 160000Lux (Major Dome & Minor dome)
➢ Controls : Control Panel (wall and on dome)
➢ Rotation : 360-330degrees
➢ Sterilizable Handle : 02Nos.
➢ Mounting Type : Ceiling
➢ Supply Voltage : 230 VAC 50 Hz
➢ Bulb Type : LED
➢ Dimming Range :50% - 100%
➢ Operating/Storage Humidity : 10 – 95%
➢ Life of Light Source :>40,000 Hrs
• Should be provision to mount the camera in one dome.
• Surgical Light System Should be European CE with 4digit notified body/US FDA certified or
Declaration of Conformity for quoted model with ISO 13485 issued by 4digit notified
body.
HD Camera System – 1080p/i.
• Description: Integrated In-Light Camera System should be integrated at the center of one of
the domes of this lighting system/third arm in order to capture images & video sequences of
the open cases.
• Such a autofocus – Lockable camera should have the following specifications -
➢ Signal to Noise Ratio (S/N Ratio) :>50 dB
➢ CCD/CMOS : 1/3‖ or1/2.8‖
➢ Optical Zoom :10X
➢ Digital Zoom :12-15X
➢ Video Output : HD, DVI, S-Video & Composite Video
➢ White Balance & Gain : Automatic/Manual
• Light and Integrated Camera should have a control through Touch Panel of the control
equipment placed inside the operating room.
• Monitors should be high definition (1920X1080p) medical grade monitor flat panel LED/LCD
with LED backlids color screen.
• The monitors should be mounted on a boom arm/Pendent/3rd arm of OT Light as suggested
by consignee/HITES the mounting accessories (if any) should be provided by bidder.
• Patch panel for power & signal to be laid down for LCD Monitors present at
Wall/Pendent/boom arm/OT Light arm by bidder.
• 3D Medical Grade Monitor ( One for each Integrated MOT)
• 26 inch or more Full High Definition (1920X1080p) medical grade monitor, flat panel LED
Colour screen to display both 2D & 3D images.
• Ceiling Boom Arm for 3D monitor–boom arm should be capable of holding 26 inch /32 inch
monitors and all fixation related work for the same should be responsibility of bidder.
• Audio Video Communication System cum control system (One for each Integrated MOT)
• The Integrate MOT should be connected to any Integrated MOT of institute (within same
building without internet connection) and can connect any Conference room/Other
MOT/Doctors lounge/Etc. for video conferencing and live transmissions through IP calling.
All necessary hardware and software should be provided by bidder.
• The Audio/Video Router/Switch system should have the minimum 8 x 8 or minimum 15
(including input & output) Digital with open architecture. The routing/Switch system should
be able to integrate and route all audio and video signal for eg. SD, Full HD & 3D signal (e.g.
Room Camera/OT Light.
• Camera/Endoscope/Microscope/Etc.) available inside OT.
• Required numbers of Decoders and Encoder or Convertors or Scalers or Transduces should be
supplied as per the respective institute requirement.
• The Integration system should receive the signal from different sources like Room camera,
Endoscopy camera, Overhead camera, Archiving System, Auxiliary devices like C-Arm,
Video Microscope, Mobile ultrasound, microphones, AUX-IN & video conferencing, etc and
able to integrate all signal and give flaxibility to route the signals/videos at desire
destination/monitors.
• The routing system should allow selection of multiple views for simultaneous transmission in
QUAD or PIP format.
• PACS dedicated PC has with trolley to be provided in each OT or integration system should
able to receive and transmit the PACS Data from source.
• Patient and image data should be able to call up and distributed to required monitors in the
operating room
• All the patch panel work required for Hardware of OT Integration system should be in the
bidder‘s scope of work and also necessary co-ordination with consignee/HITES, MOT Vendor,
construction vendor and HLL/HITES will be the responsibility of the bidder for successful
completion of the all associated works.
• Video Conferencing system should be offered and the system should be able to transfer high
quality real time images and audio signals from multipoint at a minimum speed of 2Mbps. The
system should be compatible to 1080p full HD resolution for transmission over the ISDN lines
or IP Service.
• The conferencing system should be controlled via the touch screen of the integration system
from the OT. Suitable Number / Sets of Transmitters, Receivers and Cables, connectors and
accessories should be offered as per the requirement.
• Two numbers HD camera with10x or more optical zoom should be provided in each Integrated
MOT 0as standard( One dedicated for VC & other for room view)
• Hardware for two way conferencing should be provided in each Integrated MOTs like wireless
mic, speakers, aux in and aux out & In for connecting extramic, USB/HDMI/etc. input on OT
wall panel in patch.
• Cabling for 2way conferencing between Integrated MOT to Integrated MOT within the
hospital building will be responsibility of bidder.
• Digital Documentation System (One for each Integrated MOT)
• Medical grade recorder should be provided along with monitor to display the recording/control.
• Should have provision to record FHD & 3D images and video sequences from integrated MOT.
• The Full High-Definition Digital Documentation System should be a high-end computer
system designed specifically for recording, managing, and archiving surgical images and video
in native full HD & 3D resolution. The captured full high-definition images & videos can be
accessed from the hard drive for printing or saving onto multiple forms of external media which
includes CD/DVD, USB Flash Drive & Hospital network. It should be able to preview and
simultaneously record views from two video sources parallel and archive as single patient file.
• Integration of equipment/Signals/Sources with the Central Control System in such a way that
the central control system is capable to route any running high-definition surgical videos,
which is being recorded in it, onto any display device in an operating room.
• It should have atleast 320 GB internal Hard Disk Drive (HDD) & 2 TB External online storage
for in-system archiving. Also, it should have a feature of real time in-procedure DVD burning
besides at-the- end procedure DVD burning.
• Patient and image data should be able to call up and distributed to required monitors in the
operating room
Viewer Monitor
• One 40 inch or more FHD monitor should be install on Integrated MOT wall with proper frame
(flush mounted only) and integrated with Integration system. Any image can be routed to that
monitor as per requirement. Location of this monitor will be finalized at the time of drawing
approval.
List of Approved Makes for MOT
1. Wall Paneling System SS304Make:TATA/Jindal/bhusan
2. Ceiling Paneling System SS304Make:TATA/Jindal/bhusan
3. Laminar Air Flow System Filters : AAF
4. Internal HVAC Ducting & Exhaust Al Sheet: Hindalco/TATA/Jindal/Balco
System
5. PVC Flooring Gerflor/ Tarkett
6. Hermetically Sealed Doors Metaflex
7. OT Pendants (Anesthetist & Surgeon) LMMedical/Ondal/Maquet/PneumatikBerlin
8. Peripheral lighting & Clean room Philips / Wipro / Osram/ Siska
luminaries
9. Isolation Panel System (IPS) Starstorm/ L M Medical / Bender
10. Online UPS APC/Tata Libert/Hitachi/ConsulNeowatt
11. Medical Gas Lines Installations Copper Pipe:MehtaTube(Maxflow)/Rajco/
Metal Alloys (Metalco)
Fittings : Conex Banninger
12. OT Light with camera, Monitor & Steris/ Amico / Maquet/ Stryker
Recorder
13. MOT Integration for 6 Ots Karl Storz/ Stryker /Olympus /Maquet
5 Laundry Stefab/Aquarius/Girbau
Note:
1. The contractor will use one of the approved makes as approved by the Engineer-in-charge.
2. In case of different quality/pattern of same make, the pattern/quality shall be approved Engineer
– in – charge.
3. For materials/equipment/to be used in items of work for which approved makes are not given
herein, the makes of such materials/equipment shall be as decided by Engineer–in- charge.
4. If any major equipment is using a small component of make other than that given as a Standard
component with the equipment, the same shall be accepted subject to approval of Engineer–
in-charge.
Note: All makes shall confirm to standard specification of each items as enclosed with the tender documents.
A. ALL FINISHING MATERIALS SHALL BE SELECTED IN ACCORDANCE WITH GRIHA-4 STAR
RATING REQUIREMENTS.
B. ALL GRANITE STONE AND VITRIFIED &CERAMIC TILES FLOORING SHALL BE LAID WITH
POLYMER MODIFIED ADHESIVE& JOINTING WITH 3MM EPOXY GROUT.
C. ALL SS SKIRTING SHALL BE ON 6MM THICK BACKING PLY BOARD FIXED TO THE WALL /
COLUMNS.
D. ALL LAXQUERED GLASS CLADDING SHALL HAVE BACKING OF 12MM THICK PLY BOARD.
E. AUTOCLAVED AERATED CEMENT (AAC) BLOCKS MASONRY WITH 100MM (INTERNAL) /
200MM (EXTERNAL) THICK OR AS APPROVED SIZE / THICKNESS AAC BLOCKS CONFORMING
TO IS 2185 PART 3 (1989) HAVING DENSITY IN OVEN DRY CONDITION 551-650 KG/CUM, GRADE-
I, MINIMUM COMPRESSIVE STRENGTH 4 N/MM2, THERMAL CONDUCTIVITY IN AIR DRY
CONDITION 0.23 W/MK IN SUPER STRUCTURE ABOVE PLINTH LEVEL UP TO ALL FLOOR LEVEL
AT ALL HEIGHTS, WITH RCC BAND / COLUMN AT EVERY 2.0 METRE OF PART THEREOF IN BOTH
DIRECTION, WITH APPROVED BLOCK LAYING POLYMER MODIFIED ADHESIVE MORTAR
(MINIMUM 6MM THICK) CONFORMING TO ANSI A1181 & ANSI A118.4-1999.
F. EXTERNAL / WET AREA PLASTER SHALL BE 18MM THICK (AVERAGE) READY MIX PLASTER OF
APPROVED BRAND AND MANUFACTURE SHALL BE USED AND FINISHED WITH EXTERIOR
GRADE ACRYLIC TEXTURED PAINT.
G. BARRIER FREE ACCESS SHALL BE DESIGNED AS PER NBC 2016 AND APPLICABLE
GOVERNMENT OF INDIA GUIDELINES.
H. ALL FINISHING MATERIALS SHALLBE SELECTED IN ACCORDANCE WITH GRIHA-4 STAR
RATING REQUIREMENTS.
I. INTERNAL PLASTER (except wet area) SHALL BE 12MM THICK (AVERAGE) PREMIXED
FORMULATED ONE COAT GYPSUM LIGHTWEIGHT PLASTER HAVING ADDITIVES AND LIGHT
WEIGHT AGGREGATES AS VERMICULITE / PERLITE RESPECTIVELY CONFORMING TO IS:2547
(PART I & II) 1976, APPLIED ON HACKED / UNEVEN BACKGROUND SUCH AS BARE BRICK /
BLOCK WALLS & CEILING AT ALL FLOORS AND LOCATIONS, FINISHED IN SMOOTH LINE AND
LEVEL ETC. COMPLETE.