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 - siHealth Ltd

Address:

Building R104 Rutherford Appleton Laboratory Harwell Campus

Didcot

Oxfordshire OX11 0QX

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Clinical management support software Clinical management support software Class I

Self-care monitoring/reporting software Self-care monitoring/reporting 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
Clinical management support software	Clinical management support software	Class I
Self-care monitoring/reporting software	Self-care monitoring/reporting software	Class I