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 - nal von minden GmbH

Address:

Carl-Zeiss-Strasse 12

Moers

Nordrhein-Westfalen 47445

Germany

Authorised Representative/ UK Responsible Person
Name: nal von minden Ltd
Address:

Unit 4 Gibbs Reed Farm Pashley Road

Ticehurst

East Sussex TN5 7HE

United Kingdom

Code/Term Type

Multiple drugs of abuse IVD kit rapid ICT clinical Multiple drugs of abuse IVD kit rapid ICT clinical IVD General

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.