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 Medical Products (Hangzhou) Co. Ltd.

Address:

M4-9-5 Hangzhou Economic & Technological Development Zone

Hangzhou

310018

China

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

Basic intravenous administration set invasive Basic intravenous administration set invasive Class IIa

Electric infusion pump administration set single-use Electric infusion pump administration set single-use Class IIa

Blood transfusion set non-exchange Blood transfusion set non-exchange Class IIa

Torque manipulation device Torque manipulation device 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
Basic intravenous administration set invasive	Basic intravenous administration set invasive	Class IIa
Electric infusion pump administration set single-use	Electric infusion pump administration set single-use	Class IIa
Blood transfusion set non-exchange	Blood transfusion set non-exchange	Class IIa
Torque manipulation device	Torque manipulation device	Class I