Oral/respiratory tract specimen container IVD, additive/medium - UK MHRA Medical Device Registration
Oral/respiratory tract specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 194995. The device is manufactured by DNA Genotek Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad 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
Oral/respiratory tract specimen container IVD, additive/medium
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jun 26, 2024
Name
DNA Genotek Inc.Address
3000 - 500 Palladium Drive
Ottawa, Ontario, Canada
Created Date
Jun 7, 2024
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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