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 - MedCom Gesellschaft fur medizinische Bildverarbeitung mbH

Address:

Dolivostraße 11

Darmstadt

64293

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 system application software Ultrasound imaging system application software Class IIa

Ultrasound imaging system workstation Ultrasound imaging system workstation Class I

Radiation therapy software Radiation therapy software 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
Ultrasound imaging system application software	Ultrasound imaging system application software	Class IIa
Ultrasound imaging system workstation	Ultrasound imaging system workstation	Class I
Radiation therapy software	Radiation therapy software	Class IIb