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..
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
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
Name
VISIA Lab S.r.l.Address
Via Martiri della Libertร , 95/d โ
San Giovanni Valdarno, Arezzo, Italy
Created Date
Jan 20, 2022
Relationship Type
Address
Suite 9 Cumbernauld Business Park Wardpark Road
Cumbernauld, North Lanarkshire, Scotland, United Kingdom
Postcode: G67 3JZ
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