Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - STERIS SAS

Address:

116 Avenue de Magudas Le Haillan

Bordeaux

33185

France

Authorised Representative/ UK Responsible Person
Name: STERIS Solutions Limited
Address:

Chancery House Rayns Way Watermead Business Park

Syston

Leicester

Leicestershire LE7 1PF

England United Kingdom

Code/Term Type

General utility supply system ceiling-mounted General utility supply system ceiling-mounted Class IIb

Operating room light system Operating room light system Class I

Fixed examination/treatment room light Fixed examination/treatment room light Class I

Universal operating table electromechanical Universal operating table electromechanical Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
General utility supply system ceiling-mounted	General utility supply system ceiling-mounted	Class IIb
Operating room light system	Operating room light system	Class I
Fixed examination/treatment room light	Fixed examination/treatment room light	Class I
Universal operating table electromechanical	Universal operating table electromechanical	Class I