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 - MarFlow AG

Address:

Soodstrasse 57 8134 Adliswil

Zürich

8134

Switzerland

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

Polymeric ureteral stent Polymeric ureteral stent Class IIa

Gastro-urological guidewire single-use Gastro-urological guidewire single-use Class IIa

Nephrostomy catheter introduction needle Nephrostomy catheter introduction needle Class IIa

Biliary/urinary stone retrieval basket single-use Biliary/urinary stone retrieval basket single-use Class IIa

Endoscopic-access dilator single-use Endoscopic-access dilator single-use 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
Polymeric ureteral stent	Polymeric ureteral stent	Class IIa
Gastro-urological guidewire single-use	Gastro-urological guidewire single-use	Class IIa
Nephrostomy catheter introduction needle	Nephrostomy catheter introduction needle	Class IIa
Biliary/urinary stone retrieval basket single-use	Biliary/urinary stone retrieval basket single-use	Class IIa
Endoscopic-access dilator single-use	Endoscopic-access dilator single-use	Class IIa