has been assessed and certified as meeting the requirments of
Directive 93/42/EEC
on medical devices, Annex II (excluding Section 4)
For the following product
Design & manufacture of
Medical Gas Manifold
Medical Vacuum Station
Medical Compressed Air System
Medical Gas Regulator
Medical Pendant
Medical Gas Outlet
Medical Bed Head Unit
For placiing on the market of Class III devices covered by this certificate, and EC Design Examination
Certificate according to Annex II (Section 4) is required.
This certificate is valid from 27 April 2011 until 27 April 2016 and remains
valid subject to satisfactory surveillance audits.
Re certification audit due before 31 December 2013
Issue 1. Certified since 27 April 2011