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 - Sanofi-Aventis Deutschland GmbH

Address:

Industriepark Hoechst

Frankfurt am Main

65926

Germany

Authorised Representative/ UK Responsible Person
Name: Aventis Pharma Limited trading as Sanofi
Address:

410 Thames Valley Park Earley

Reading

RG6 1PT

England United Kingdom

Code/Term Type

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Class IIb

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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