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 - Guangzhou iCare Medical Technology Co. Ltd.

Address:

First Floor A No. 8 Lianhua Port Industrial Zone Lotus Mountain Bonded Area Shilou Town

Panyu District

Shilou Town

Guangzhou 511440

China

Authorised Representative/ UK Responsible Person
Name: BETACHEK (UK) LIMITED
Address:

7 Bell Yard

London

WC2A 2JR

England United Kingdom

Code/Term Type

Blood lancet single-use Blood lancet 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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