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 - Livetec Ingenieursbuero GmbH

Address:

Marie-Curie-Strasse 8

Loerrach

79539

Germany

Authorised Representative/ UK Responsible Person
Name: UK Doctors Ltd
Address:

1 The Powdermills Old Malden Lane

Worcester Park

Surrey KT4 7PZ

England United Kingdom

Code/Term Type

Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Class IIa

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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