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

Back to MHRA

Manufacturer's Devices - NE Device SW Oy

Address:

Teknologiantie 7b

Oulu

90590

Finland

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

The Health And Wellbeing Innovation Centre

Truro

Cornwall TR1 3FF

England United Kingdom

Code/Term Type

Cardiopulmonary parameter spot-check measurement software Cardiopulmonary parameter spot-check measurement software 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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