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 - KINVENT Biomecanique SAS

Address:

Cap omega - cs 39521

Montpellier

Rond-point Benjamin Franklin 34000

France

Authorised Representative/ UK Responsible Person
Name: ALS International Ltd Trading as I3CGLOBAL(UK)
Address:

Office 54 58 Peregrine Road

Hainault

Ilford

Essex IG6 3SZ

England United Kingdom

Code/Term Type

Electronic goniometer/kinesiology sensor Electronic goniometer/kinesiology sensor Class I

Hand dynamometer/pinchmeter electronic Hand dynamometer/pinchmeter electronic Class I

Back/leg/chest dynamometer electronic Back/leg/chest dynamometer electronic Class I

Biomechanical function analysis system force-testing portable Biomechanical function analysis system force-testing portable 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
Electronic goniometer/kinesiology sensor	Electronic goniometer/kinesiology sensor	Class I
Hand dynamometer/pinchmeter electronic	Hand dynamometer/pinchmeter electronic	Class I
Back/leg/chest dynamometer electronic	Back/leg/chest dynamometer electronic	Class I
Biomechanical function analysis system force-testing portable	Biomechanical function analysis system force-testing portable	Class I