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 - AB Medica Group S.A.

Address:

Llobateras 14-18 Talleres 7 Nave 4 Polígono Industrial Salvatella

Barberà del Vallès

Barcelona 8210

Spain

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

34 Anyards Road

Cobham

Surrey KT 11 2LA

England United Kingdom

Code/Term Type

Echocardiographic recording paper Echocardiographic recording paper Class I

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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