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 - VISIA Lab S.r.l.

Address:

Via Martiri della Libertà 95/d –

San Giovanni Valdarno

Arezzo 52027

Italy

Authorised Representative/ UK Responsible Person
Name: QCS International LTD.
Address:

Suite 9 Cumbernauld Business Park

Wardpark Road

Cumbernauld

North Lanarkshire G67 3JZ

Scotland United Kingdom

Code/Term Type

Fluorescent immunoassay analyser IVD laboratory semi-automated Fluorescent immunoassay analyser IVD laboratory semi-automated 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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