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

Back to MHRA

Manufacturer's Devices - My Med Kft

Address:

Vendel utca 11

Budapest

Budapest

Budapest 1096

Hungary

Authorised Representative/ UK Responsible Person
Name: Insight Regulatory Consultancy Ltd.
Address:

Unit A Wixford Park George's Elm Lane

Bidford on Avon

Alcester

Warwickshire B50 4JS

England United Kingdom

Code/Term Type

Dermal tissue reconstructive material microbe-derived Dermal tissue reconstructive material microbe-derived Class III

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.