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 - Shenzhen Superline Technology Co. Ltd.

Address:

Room 1206 Building 4 Chongwen Garden

Taoyuan Street Nanshan District

Shenzhen

Guangdong 518055

China

Authorised Representative/ UK Responsible Person
Name: B D S I Ltd
Address:

Unit 14 Cannon Way

Barnsley

South Yorkshire S75 1JU

England United Kingdom

Code/Term Type

Endodontic broach serrated single-use Endodontic broach serrated single-use Class IIa

Rotary/reciprocating endodontic file/rasp single-use Rotary/reciprocating endodontic file/rasp single-use 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
Endodontic broach serrated single-use	Endodontic broach serrated single-use	Class IIa
Rotary/reciprocating endodontic file/rasp single-use	Rotary/reciprocating endodontic file/rasp single-use	Class IIa