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 Surya Binayak Nagar Hospital
Bhaktapur
MEDICAL GAS PIPELINE AND ACCESSORIES CALCULATION

S. N Technical Specification Unit Quantity Remarks

Copper pipes used shall be half drawn, tampered,
seamless and manufactured from phosphorous
deoxidised (non-arsenical) copper alloy CW024A.
The chemical composition being CU.DHP to ISO
1190-1/CW024A to EN1412. Degreased copper
tube and fittings should be manufactured under BS
EN 13485 Medical Devices: Quality Management
Systems. Degreased copper tubes should be CE
marked as Class IIa Medical Device under Medical
Device Directive 93/42/EEC.

Copper Fittings should be manufactures under BS

EN 13485 Medical Devices: Quality Management
1
Systems and should be suitable for jointing
degreased medical copper tubes. Brass Saddles
should be suitable for suspending copper tube with
metric threaded studding or screws.

All copper tube of all sizes should be

engraved/permanently ink marked with the
following information:
Harmonised standard number EN 13348, nominal
dimensions (OD x thickness), manufacturer details,
CE Mark (CE 0086), medical (Medical Device
Directive to 93/42/EEC), time and date of
production.
1.1 15 mm OD x 0.6 mm thick Meter 208
1.2 22 mm OD x 0.7 mm thick Meter 169
1.3 28 mm OD x 0.9 mm thick Meter 213
1.4 UPVC Pipe Meter 213
2 Gas Outlet Points (Terminal Units):
Medical gas Outlet points must be simple design
straight forward to install and smooth in operation.
The gas terminal unit should be 100% all metal
construction. All terminal units must have stainless
steel rolling pins that allow the smooth insertion and
removal of probes. The different gases should be
clearly identified on the ring socket by the use of bold
permanent colours. Gas Terminal Units should have
cleanliness below 0.01 mg/cm² of hydrocarbons on the
degreased surface of the product. Medical gas terminal
units shall fully comply with the requirements of the
UK DoH Health Technical Memorandum HTM2022
and HTM 02-01. Medical gas terminal units shall be
 CE marked to the Medical Device Directive 93/43/EC
as a class IIb medical device with notified body
British Standards Institute (BSI). CE mark should be
specified on the ring socket of outlet as well.
2.1 Oxygen Set 33
2.2 Vacuum Set 27
2.3 Oxygen valve Set 25
2.4 Air Set 15
Oxygen flow meter with humidifier bottle:
Pressure compensated flow meter should be of
accurate gas flow measurement and control within a
range of 0-15 LPM for use in a variety of
respiratory therapy gas delivery system. The flow
3 tube and shroud components should be made of Set 33
good quality polycarbonate. Humidifier bottle
should also be made of unbreakable clear
polycarbonate material and reusable after
disinfection, it should be auto-cleavable. Complete
set should be CE certified.
Suction Collection Jars
Suction Collection Jars of volume minimum 1500
ml should be made of transparent polycarbonate
materials autoclavable at min. 121℃. It should
have a positive shut-off cap and float assembly to
interrupt suction to prevent fluid carryover into
the regulator. It should have removable plastic
4 bracket with hose barb connection for connecting Set 27
with Vacuum regulator and patient connecting
tube.
It should be supplied with non-toxic, non-irritant,
medical grade. Pressure resistant PVC connecting
tubes of length 150 cm.
It should be supplied with aluminum slide bracket
and plastic bottle hanger.
Fitting accessories Installation charge
All Required T, Elbow, Reducer, Reducer Elbow
5 Grip. Clamp, saddle, screw, etc. as per site Lot 1
requirement during installation including
installation charge

For Hospi Solution Pvt. Ltd.

……………………………
Mukund Khatiwada
Biomedical Engineer