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 - Etex Corporation

Address:

55 Messina Drive

Braintree

MA 02184

United States

Authorised Representative/ UK Responsible Person
Name: Zimmer Biomet UK Limited
Address:

Stella Building Windmill Hill Business Park

Whitehill Way

Swindon

SN5 6NX

England United Kingdom

Code/Term Type

Synthetic bone graft Synthetic bone graft Class III

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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