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 - Neoventa Medical AB

Address:

Norra Ågatan 32

Mölndal

43135

Sweden

Authorised Representative/ UK Responsible Person
Name: Neoventa Medical Ltd
Address:

34 Anyards Road

Cobham

Surrey KT 11 2LA

England United Kingdom

Code/Term Type

Electrocardiographic lead set reusable Electrocardiographic lead set reusable Class I

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.