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 - GfM mbH

Address:

Wasserweg 19

Groß-Gerau

64521

Germany

Authorised Representative/ UK Responsible Person
Name: UKCApartner4U Limited
Address:

7 CAMPION WAY

BINGHAM NOTTINGHAM

NG13 8 TR

England United Kingdom

Code/Term Type

Ultrasound imaging transducer positioning unit Ultrasound imaging transducer positioning unit Class I

Needle guide single-use Needle guide single-use Class I

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
Ultrasound imaging transducer positioning unit	Ultrasound imaging transducer positioning unit	Class I
Needle guide single-use	Needle guide single-use	Class I