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 - Tianjin Huahong Technology Co. Ltd.

Address:

A01 Plant B No. 278 Hangkong Road Tianjin Pilot Free Trade Zone(Air Port Industrial Park)

Tianjin

300308

China

Authorised Representative/ UK Responsible Person
Name: lotus global co ltd
Address:

23 Maine Street

Reading

Reading RG2 6AG

England United Kingdom

Code/Term Type

Manual blood lancing device reusable Manual blood lancing device reusable Class I

Blood lancing device tip Blood lancing device tip Class IIa

Manual blood lancing device single-use Manual blood lancing device single-use Class IIa

Autoinjector needle Autoinjector needle 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
Manual blood lancing device reusable	Manual blood lancing device reusable	Class I
Blood lancing device tip	Blood lancing device tip	Class IIa
Manual blood lancing device single-use	Manual blood lancing device single-use	Class IIa
Autoinjector needle	Autoinjector needle	Class IIa