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 - 3D-Side

Address:

5 Rue André Dumont

Mont-Saint-Guibert

Nivelles

Brabant Wallon 1435

Belgium

Authorised Representative/ UK Responsible Person
Name: AJSA Consulting Ltd
Address:

32 Meadow Drive

Knutsford

Cheshire WA16 0DT

England United Kingdom

Code/Term Type

Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide

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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