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 - Nipro Renal Solutions Spain S.L.U.

Address:

Pol. Ind. Tumsa nave no 31

Mollerussa

Lleida E-25230

Spain

Authorised Representative/ UK Responsible Person
Name: Nipro Medical UK Ltd
Address:

Units 12-14 South Point Ensign Way

Hamble-Le-Rice

Southampton

Hampshire SO31 4RF

England United Kingdom

Code/Term Type

Haemodialysis concentrate Haemodialysis concentrate 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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