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Fluorescent immunoassay analyser IVD, laboratory, semi-automated - UK MHRA Medical Device Registration

Fluorescent immunoassay analyser IVD, laboratory, semi-automated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 133369. The device is manufactured by VISIA Lab S.r.l. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is QCS International LTD..

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In Vitro Diagnostic Device
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Fluorescent immunoassay analyser IVD, laboratory, semi-automated
MHRA Device ID: 133369โ€ขRef: 133369

Device Type

In Vitro Diagnostic Device

Devices

Fluorescent immunoassay analyser IVD, laboratory, semi-automated

Type

IVD General

Date Registered

Nov 19, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Address

Via Martiri della Libertร , 95/d โ€“

San Giovanni Valdarno, Arezzo, Italy

Created Date

Jan 20, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Suite 9 Cumbernauld Business Park Wardpark Road

Cumbernauld, North Lanarkshire, Scotland, United Kingdom

Postcode: G67 3JZ

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