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 - Physidia SAS

Address:

11-13 Bd des Bretonnieres

Saint-Barthelemy d'Anjou

49124

France

Serilization:

Authorised Representative
Name: Xtra-med Ltd
Address:

Thorneycroft Farm

Kettleshulme

SK23 7RG

England United Kingdom

Code/Term Type

Haemodialysis blood tubing set, single-use Class IIa

Haemodialysis system, institutional/home-use Class IIb

Haemodialysis system dialysate delivery set Class IIa

Intravenous pole Class I

Haemodialysis dialysate solution 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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Code/Term		Type
Haemodialysis blood tubing set, single-use		Class IIa
Haemodialysis system, institutional/home-use		Class IIb
Haemodialysis system dialysate delivery set		Class IIa
Intravenous pole		Class I
Haemodialysis dialysate solution		Class IIb