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 - Corporation STERIS Canada

Address:

490 Boulevard Armand-Paris

Québec

Québec G1C 8A3

Canada

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

Endoscope washer/disinfector Endoscope washer/disinfector Class IIb

Luminal device flushing tubing set reusable Luminal device flushing tubing set reusable Class I

Surgical utensil washer/disinfector Surgical utensil washer/disinfector Class IIb

Invasive medical device leak tester mechanical Invasive medical device leak tester mechanical Class I

Invasive medical device leak tester mechanical Invasive medical device leak tester mechanical 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
Endoscope washer/disinfector	Endoscope washer/disinfector	Class IIb
Luminal device flushing tubing set reusable	Luminal device flushing tubing set reusable	Class I
Surgical utensil washer/disinfector	Surgical utensil washer/disinfector	Class IIb
Invasive medical device leak tester mechanical	Invasive medical device leak tester mechanical	Class I
Invasive medical device leak tester mechanical	Invasive medical device leak tester mechanical	Class I