Laboratory instrument/analyser application software IVD - UK MHRA Medical Device Registration
Laboratory instrument/analyser application software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 127381. The device is manufactured by CellaVision AB from Sweden, classified as In Vitro Diagnostic Device. The authorized representative in the UK is QAdvis UK 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
Laboratory instrument/analyser application software IVD
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 2, 2024
Name
QAdvis UK LtdRelationship Type
Address
55-66 Frederick Street
Edinburgh, EH2 1LS, Scotland, United Kingdom
Postcode: EH2 1LS
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Registered: Nov 26, 2024
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Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Cell morphology analyser IVD, automated/semi-automated
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Cell morphology analyser IVD, automated/semi-automated
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Laboratory instrument/analyser application software IVD
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Cell morphology analyser IVD, automated/semi-automated
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Laboratory instrument/analyser application software IVD
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Laboratory instrument/analyser application software IVD
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Cell morphology analyser IVD, automated/semi-automated
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
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