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 - Cardisio GmbH

Address:

The Squaire 12

Frankfurt-am-Main

D-60549

Germany

Authorised Representative/ UK Responsible Person
Name: Heartwave Limited
Address:

20-22 Wenlock Road

London

N1 7GU

England United Kingdom

Code/Term Type

Cardiology information system application software Cardiology information system application software 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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