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 - Sun Medical Co. Ltd.

Address:

571-2 Furutaka-Cho,,,

Moriyama

Shiga 524-0044,

Japan

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Dental composite resin kit Dental composite resin kit Class IIa

Dental material application tool single-use Dental material application tool single-use Class I

Dappen dish holder Dappen dish holder Class I

Dappen dish single-use Dappen dish single-use Class I

Dental material injection cannula single-use Dental material injection cannula single-use Class I

Dental material application tool reusable Dental material application tool reusable 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
Dental composite resin kit	Dental composite resin kit	Class IIa
Dental material application tool single-use	Dental material application tool single-use	Class I
Dappen dish holder	Dappen dish holder	Class I
Dappen dish single-use	Dappen dish single-use	Class I
Dental material injection cannula single-use	Dental material injection cannula single-use	Class I
Dental material application tool reusable	Dental material application tool reusable	Class I