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 - DENTECH CORPORATION

Address:

53-5 Shimizu-cho Itabashi-ku

Tokyo

174-0053

Japan

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Rubber dam non-latex Rubber dam non-latex Class I

Rubber dam frame Rubber dam frame Class I

Rubber dam kit Rubber dam kit Class I

Rubber dam clamp Rubber dam clamp Class I

Rubber dam Hevea-latex Rubber dam Hevea-latex Class I

Rubber dam punch Rubber dam punch Class I

Rubber dam clamp forceps Rubber dam clamp forceps 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
Rubber dam non-latex	Rubber dam non-latex	Class I
Rubber dam frame	Rubber dam frame	Class I
Rubber dam kit	Rubber dam kit	Class I
Rubber dam clamp	Rubber dam clamp	Class I
Rubber dam Hevea-latex	Rubber dam Hevea-latex	Class I
Rubber dam punch	Rubber dam punch	Class I
Rubber dam clamp forceps	Rubber dam clamp forceps	Class I