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.
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Manufacturer's By Device Cardiac transseptal access electrosurgical dilator/needle-Cardiac transseptal access electrosurgical dilator/needle
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
Acutus Medical Inc.
2210 Faraday Avenue Suite 100
Carlsbad
California 92008
United States
Acutus Medical UK Limited
Hill House 1 Little New Street
London
EC1A 3TR
England United Kingdom
03/18/2023
24377