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 Inc trading as Baxter Opelika

Address:

1101 Jeter Avenue

Alabama

Opelika AL 36801

United States

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

Caxton Way

Thetford

Norfolk IP24 3SQ

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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