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 - Chengdu OCI Medical Devices Co. Ltd

Address:

No. 2401 West Port Avenue Southwest Airport Economic Development Zone

Shuangliu District

Chengdu

Sichuan Province 610299

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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