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 - Brainlab Ltd.

Address:

35 Efal Street

Petah Tikva

Central 4951132

Israel

Authorised Representative/ UK Responsible Person
Name: Brainlab Limited
Address:

C/O Booth Parkes & Assoc Ltd Southolme Trinity Street

Gainsborough

Lincolnshire DN21 2EQ

England United Kingdom

Code/Term Type

Orthopaedic/craniofacial implantation planning software Orthopaedic/craniofacial implantation planning software 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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