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 - ProWellness Health Solutions Oy

Address:

Hoitajanrinne 1 D

Oulu

90220

Finland

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

17 Alvaston Business Park Middlewich Road

Nantwich Cheshire

Nantwich

Cheshire CW5 6PF

England United Kingdom

Code/Term Type

Home pharmaceutical management support software Home pharmaceutical management support software Class IIb

Self-care monitoring/reporting software Self-care monitoring/reporting software Class I

Configurable electronic form web-based application software Configurable electronic form web-based 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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Code/Term		Type
Home pharmaceutical management support software	Home pharmaceutical management support software	Class IIb
Self-care monitoring/reporting software	Self-care monitoring/reporting software	Class I
Configurable electronic form web-based application software	Configurable electronic form web-based application software	Class I