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 (Philippines) Corporation

Address:

124 East Main Avenue Laguna Technopark Binan

Laguna

4024

Philippines

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

Metered-delivery hypodermic syringe Metered-delivery hypodermic syringe Class IIa

General-purpose syringe/needle General-purpose syringe/needle Class IIa

Hypodermic needle single-use Hypodermic needle single-use Class IIa

Insulin syringe/needle basic Insulin syringe/needle basic Class IIa

Peripheral intravenous cannula Peripheral intravenous cannula Class IIa

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
Metered-delivery hypodermic syringe	Metered-delivery hypodermic syringe	Class IIa
General-purpose syringe/needle	General-purpose syringe/needle	Class IIa
Hypodermic needle single-use	Hypodermic needle single-use	Class IIa
Insulin syringe/needle basic	Insulin syringe/needle basic	Class IIa
Peripheral intravenous cannula	Peripheral intravenous cannula	Class IIa