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 - Suzhou ZOEY Medical Devices Co Ltd.

Address:

2nd Floor Building 18 Guanpu Road No. 333 Guoxiang Street

Wuzhong Economic Development Zone

Suzhou

215100

China

Authorised Representative/ UK Responsible Person
Name: LUNDATEC UK LTD
Address:

First Floor 12 Commerce Road Lynch Wood

Peterborough

Cambridgeshire PE2 6LR

England United Kingdom

Code/Term Type

Hollow-fibre haemodialysis dialyser single-use Hollow-fibre haemodialysis dialyser single-use Class IIb

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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