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

Back to MHRA

Manufacturer's Devices - Shenzhen Dakewe Bio-engineering Co. Ltd.

Address:

Room 702-703 Building No.1 Shenzhen Biomedicine Innovations Industrial Park No.14 Jinhui Road Kengzi Street Pingshan District

Shenzhen Guangdong

518122

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

General specimen container IVD additive/medium General specimen container IVD additive/medium IVD General

General specimen collection kit IVD clinical General specimen collection kit IVD clinical IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
General specimen container IVD additive/medium	General specimen container IVD additive/medium	IVD General
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	IVD General