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 - Studioemme SAS

Address:

Via della Salute 18/9

Bologna

40132

Italy

Authorised Representative/ UK Responsible Person
Name: Dentsply IH Limited
Address:

Building 3 The Heights Brooklands

Weybridge

Surrey KT13 0NY

England United Kingdom

Code/Term Type

Orthodontic tube Orthodontic tube Class IIb

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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