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 - Disior Oy

Address:

Ruusutarhantie 7 A

Helsinki

00300

Finland

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

3 Oak Court Pilgrims Walk

Prologis Park

Coventry

CV6 4QH

England United Kingdom

Code/Term Type

CAD/CAM software CAD/CAM software Class IIb

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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Code/Term		Type
CAD/CAM software	CAD/CAM software	Class IIb
Orthopaedic/craniofacial implantation planning software	Orthopaedic/craniofacial implantation planning software	Class I