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 - PulseOn Oy

Address:

Tekniikantie

Espoo

Espoo

02150

Finland

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

The Stables Overton

Ashover

Chesterfield

Derbyshire S45 0JR

England United Kingdom

Code/Term Type

Cardiac arrhythmia monitoring system Cardiac arrhythmia monitoring system 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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