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 - FLUOPTICS SAS

Address:

Rue des berges 44

Grenoble

38000

France

Authorised Representative/ UK Responsible Person
Name: Medes Ltd.
Address:

5 Beaumont Gate Shenley Hil

Radlett

Herts WD77AR

England United Kingdom

Code/Term Type

Frame/rail/pole device holder Frame/rail/pole device holder Class I

Electromechanical device/system transport trolley Electromechanical device/system transport trolley Class I

Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Conformity Assessment Certificate Expired Class IIa

Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera 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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Code/Term		Type
Frame/rail/pole device holder	Frame/rail/pole device holder	Class I
Electromechanical device/system transport trolley	Electromechanical device/system transport trolley	Class I
Diagnostic-imaging multiformat camera	Diagnostic-imaging multiformat camera Conformity Assessment Certificate Expired	Class IIa
Diagnostic-imaging multiformat camera	Diagnostic-imaging multiformat camera	Class IIa