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 - Finapres Medical Systems BV

Address:

Institutenweg 25

Enschede

7521 PH

Netherlands

Authorised Representative/ UK Responsible Person
Name: SMART Medical Limited
Address:

Kenton House Oxford Street

Moreton-in-Marsh

Gloucestershire GL56 0LA

England United Kingdom

Code/Term Type

Patient monitoring system module blood pressure noninvasive Patient monitoring system module blood pressure noninvasive 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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