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 - Gambro Renal Products S.A. de C.V. trading as Baxter Tijuana

Address:

Boulevard Pacifico No. 10014 Parque Industrial Pacifico

Tijuana

Baja California C.P. 22643

Mexico

Authorised Representative/ UK Responsible Person
Name: Baxter Healthcare Ltd
Address:

Caxton Way

Thetford

Norfolk IP24 3SQ

England United Kingdom

Code/Term Type

Haemodialysis blood tubing set single-use Haemodialysis blood tubing set 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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