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 - Laboratorios Grifols SA

Address:

Poligono Levante Can Guasch s/n

Parets del Valles

Barcelona

08150

Spain

Authorised Representative/ UK Responsible Person
Name: Grifols UK Limited
Address:

3980-3990 Enterprise Cambridge Research Park

Beach Drive

Waterbeach

CB25 9PE

England United Kingdom

Code/Term Type

Red blood cell separation reagent Red blood cell separation reagent Class IIb

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

Intravenous administration bag/bottle Intravenous administration bag/bottle 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
Red blood cell separation reagent	Red blood cell separation reagent	Class IIb
Fluid transfer set general-purpose	Fluid transfer set general-purpose	Class I
Intravenous administration bag/bottle	Intravenous administration bag/bottle	Class I