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Medical Gas Outlets

Medical Gas Outlets
Medical Gas Outlets
Product Code : 04
Brand Name : IOMS
Product Description

Our relentless hard work and rich knowledge helps us in offering stellar quality Gas Outlet to our treasured clients. This product is used for ensuring connectivity to secondary devices like suction equipment, oxygen therapy unit, medical Pneumatic Saw, air motor operation and Ventilators. The offered product is manufactured under the stern observation of vendor’s highly knowledgeable professionals using admirable quality raw materials and pioneering technology. Moreover, this Gas Outlet is available in various specifications as per the precise needs of clients and at market leading prices.


  • Fine finish

  • Light weight

  • Durability

  • Easy to fit


Interfacing the secondary devices with the outlet (Terminal Units) of the Indo Omex is extremely important for safety and effective functioning of the devices.
Indo Omex’s easy to connect with gas specific probe ensure connectivity solution to secondary devices i.e. Oxygen therapy unit, Suction equipment, Air motor operation, Ventilators, Medical Pneumatic Saw, Drill etc.

Outlets shall be manufactured with a 6 - 1/2" [165 mm] length type "K" 1/2" [12.7 mm] outside diameter (3/8" nominal) size copper inlet pipe stub, which is silver brazed to the outlet body. The body shall be of 1-5/16" [33 mm] diameter, one piece brass construction. For positive pressure gas services, the outlet shall be equipped with a primary and secondary check valve and the secondary check valve shall be rated at a maximum of 200 psi [1,379 kPa] in the event the primary check valve is removed for maintenance. Outlet bodies shall be gas specific by indexing each gas service to a gas specific dual pin indexing arrangement on the respective identifica- tion module.

A large color coded front plate shall be used for ease of gas identification and aesthetic appeal.

The secondary device interfacing solution of INDO OMEX is simple, safe, secure and effective. The solution offered meets the requirements of the Directive 93/42/EEC concerning medical devices and the amendment introduced by directive 2007 / 47/ EC.