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 - CardioTek B.V.

Address:

Dr. Nolenslaan 107 B

Dr. Nolenslaan Sittard

Sittard-Geleen

Limburg 6136 GL

Netherlands

Authorised Representative/ UK Responsible Person
Name: RLD Quality Limited
Address:

Centenary House Peninsula Park

Rydon Lane

Exeter

Devon EX2 7XE

England United Kingdom

Code/Term Type

Cardiac electrophysiology analysis system Cardiac electrophysiology analysis system Class IIb

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.