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 - iLsa Diagnostic

Address:

Rue de la comtesse

Marchaux

F.25640

France

Authorised Representative/ UK Responsible Person
Name: Pro-Lab Diagnostics
Address:

3 Bassendale Road

Bromborough

Wirral CH62 3QL

England United Kingdom

Code/Term Type

Clinical laboratory analyser/instrument control unit IVD Clinical laboratory analyser/instrument control unit IVD IVD General

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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