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 - Biogen MA Inc.

Address:

225 Binney Street

Cambridge

MA MA 02142

United States

Authorised Representative/ UK Responsible Person
Name: Biogen Idec Limited
Address:

Innovation House 70 Norden Rd

Maidenhead

Berkshire SL64AY

England United Kingdom

Code/Term Type

Syringe plunger stop Syringe plunger stop 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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