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 Corporation

Address:

950 Elkton Boulevard

Elkton

Maryland 21921

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

Vascular catheter introduction set nonimplantable Vascular catheter introduction set nonimplantable Class IIa

Tourniquet cuff single-use Tourniquet cuff single-use Class I

Vascular guide-catheter single-use Vascular guide-catheter single-use Class III

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
Vascular catheter introduction set nonimplantable	Vascular catheter introduction set nonimplantable	Class IIa
Tourniquet cuff single-use	Tourniquet cuff single-use	Class I
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class III