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 - Naviswiss AG

Address:

Stahlrain 2 CH-5200

Brugg

5200

Switzerland

Authorised Representative/ UK Responsible Person
Name: confinis (UK) RP Ltd
Address:

St John's Innovation Centre Cowley Road

Cambridge

CB4 0WS

England United Kingdom

Code/Term Type

Orthopaedic/craniofacial implantation planning software Orthopaedic/craniofacial implantation planning software Class I

Optical surgical navigation device tracking system Optical surgical navigation device tracking system Class IIa

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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Code/Term		Type
Orthopaedic/craniofacial implantation planning software	Orthopaedic/craniofacial implantation planning software	Class I
Optical surgical navigation device tracking system	Optical surgical navigation device tracking system	Class IIa