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 Inc

Address:

100 Route 206 North

Peapack

New Jersey 07977

United States

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

Self-care monitoring/reporting software Self-care monitoring/reporting software Class I

Clinical training/education software Clinical training/education software Class I

Pharmaceutical management support software professional-use Pharmaceutical management support software professional-use 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
Self-care monitoring/reporting software	Self-care monitoring/reporting software	Class I
Clinical training/education software	Clinical training/education software	Class I
Pharmaceutical management support software professional-use	Pharmaceutical management support software professional-use	Class I