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 - Terumo Cardiovascular Systems Corporation

Address:

6200 Jackson Road

Ann Arbor

Michigan 48103

United States

Authorised Representative/ UK Responsible Person
Name: Terumo UK Ltd
Address:

Otium House 2 Freemantle Road

Bagshot

Surrey GU19 5LL

England United Kingdom

Code/Term Type

Extracorporeal blood gas/pH monitor Extracorporeal blood gas/pH monitor Class IIb

Medical device service rail clamp Medical device service rail clamp Class I

Cardiopulmonary bypass system air bubble/fluid level detector Cardiopulmonary bypass system air bubble/fluid level detector 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
Extracorporeal blood gas/pH monitor	Extracorporeal blood gas/pH monitor	Class IIb
Medical device service rail clamp	Medical device service rail clamp	Class I
Cardiopulmonary bypass system air bubble/fluid level detector	Cardiopulmonary bypass system air bubble/fluid level detector	Class I