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 - 3DIEMME Srl

Address:

Via Risorgimento 0

Cantu

22063

Italy

Authorised Representative/ UK Responsible Person
Name: Biomet 3i UK Ltd
Address:

1 Glass Wharf Burges Salmon Rep Office

Bristol

BS2 0ZX

England United Kingdom

Code/Term Type

Dental implantation drilling template guide-sleeve Dental implantation drilling template guide-sleeve Class I

CAD/CAM software CAD/CAM software 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
Dental implantation drilling template guide-sleeve	Dental implantation drilling template guide-sleeve	Class I
CAD/CAM software	CAD/CAM software	Class IIa