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

Authorised Representative/ UK Responsible Person
Name: Xtra-med Ltd
Address:

Thorneycroft Farm

Kettleshulme

SK23 7RG

England United Kingdom

Code/Term Type

Haemodialysis blood tubing set single-use Haemodialysis blood tubing set single-use Class IIa

Haemodialysis system institutional/home-use Haemodialysis system institutional/home-use Class IIb

Haemodialysis system dialysate delivery set Haemodialysis system dialysate delivery set Class IIa

Intravenous pole Intravenous pole Class I

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