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

Back to MHRA

Manufacturer's Devices - HyperBranch Medical Technology Inc.

Address:

800-12 Capitola Dr

Durham

27713

United States

Authorised Representative/ UK Responsible Person
Name: Stryker UK Ltd
Address:

Stryker House Hambridge Road

Newbury

Berkshire RG14 5AW

England United Kingdom

Code/Term Type

Dura mater sealant Dura mater sealant 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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