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 - pfm medical mepro gmbh

Address:

Am Soterberg 4

66620 Nonnweiler

66620

Germany

Authorised Representative/ UK Responsible Person
Name: pfm medical UK Limited
Address:

Suite 3 Armcon Business Park London Road South

Poynton

Cheshire SK12 1LQ

England United Kingdom

Code/Term Type

Vascular port/catheter Vascular port/catheter Class IIa

Cardiac defect occluder Cardiac defect occluder Class III

Pleural/peritoneal drainage catheterization kit Pleural/peritoneal drainage catheterization kit Class IIa

Peripheral intravenous cannula Peripheral intravenous cannula Class IIa

Closed-wound drainage kit Closed-wound drainage kit Class IIa

Vascular catheter introduction set nonimplantable Vascular catheter introduction set nonimplantable 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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Code/Term		Type
Vascular port/catheter	Vascular port/catheter	Class IIa
Cardiac defect occluder	Cardiac defect occluder	Class III
Pleural/peritoneal drainage catheterization kit	Pleural/peritoneal drainage catheterization kit	Class IIa
Peripheral intravenous cannula	Peripheral intravenous cannula	Class IIa
Closed-wound drainage kit	Closed-wound drainage kit	Class IIa
Vascular catheter introduction set nonimplantable	Vascular catheter introduction set nonimplantable	Class IIa