Influenza A virus H1N1 subtype (swine influenza) nucleic acid IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration
Influenza A virus H1N1 subtype (swine influenza) nucleic acid IVD, kit, nucleic acid technique (NAT) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135831. The device is manufactured by TIB Molbiol Syntheselabor Gmbh from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Roche Diagnostics Limited.
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
Influenza A virus H1N1 subtype (swine influenza) nucleic acid IVD, kit, nucleic acid technique (NAT)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Nov 15, 2024
Address
Eresburgstraรe 22โ23
Berlin, Germany
Created Date
Feb 9, 2022
Relationship Type
Address
Roche Diagnostics Limited Charles Avenue
Burgess Hill, West Sussex, United Kingdom
Postcode: RH15 9RY
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Type: In Vitro Diagnostic Device
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BK virus (BKV) nucleic acid IVD, kit, nucleic acid technique (NAT)
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Buffered wash solution IVD
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