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 - Pfizer Manufacturing Belgium NV

Address:

Rijksweg 12

Puurs

2870

Belgium

Authorised Representative/ UK Responsible Person
Name: Pfizer R&D UK Ltd
Address:

Discovery Park Ramsgate Road

Sandwich

Kent CT13 9NJ

England United Kingdom

Code/Term Type

Needle guard Needle guard Class I

Subcutaneous self-injection aid Subcutaneous self-injection aid Class I

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Conformity Assessment Certificate Expired 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
Needle guard	Needle guard	Class I
Subcutaneous self-injection aid	Subcutaneous self-injection aid	Class I
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical Conformity Assessment Certificate Expired	Class IIa