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

Back to MHRA

Manufacturer's Devices - Shire Human Genetic Therapies Inc. (Shire HGT)

Address:

300 Shire Way

Lexington

MA 02421

United States

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Class IIa

Coagulation factor VIII IVD antibody Coagulation factor VIII IVD antibody IVD General

Fluid transfer set general-purpose Fluid transfer set general-purpose Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Subcutaneous infusion/injection port needle	Subcutaneous infusion/injection port needle	Class IIa
Coagulation factor VIII IVD antibody	Coagulation factor VIII IVD antibody	IVD General
Fluid transfer set general-purpose	Fluid transfer set general-purpose	Class I