United Kingdom MHRA device registration 133369

Fluorescent immunoassay analyser IVD, laboratory, semi-automated

United Kingdom·In Vitro Diagnostic Device·VISIA Lab S.r.l.·Registered Nov 19, 2024

Registration details

Device ID: 133369
MHRA Reference Number: 133369
Date Registered: Nov 19, 2024
Last Updated: Oct 31, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Fluorescent immunoassay analyser IVD, laboratory, semi-automated
Type: IVD General

Manufacturer

Name: VISIA Lab S.r.l.
Address: Via Martiri della Libertà, 95/d –
San Giovanni Valdarno, Arezzo, Italy
Created Date: Jan 20, 2022

Authorized Representative

Name: QCS International LTD.
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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About this record

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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