Human bocavirus (HBoV) nucleic acid IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration
Human bocavirus (HBoV) 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 214134. The device is manufactured by TIB Molbiol Syntheselabor Gmbh from Germany, classified as In Vitro Diagnostic Device.
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Device Type
In Vitro Diagnostic Device
Type
IVD General
Status
Date Registered
Mar 25, 2025
Address
Eresburgstraรe 22โ23
Berlin, Germany
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Type: In Vitro Diagnostic Device
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Type: In Vitro Diagnostic Device
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Type: In Vitro Diagnostic Device
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Type: In Vitro Diagnostic Device
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Multiple inborn immunodeficiency/muscular/haematological disorder IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Mar 25, 2025
Multiple human parainfluenza virus nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Mar 25, 2025
Angiotensin converting enzyme (ACE) gene polymorphism IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Mar 25, 2025
Alpha-1-antitrypsin deficiency IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Fructose/lactose intolerance IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Human metapneumovirus (hMPV) nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Dengue virus nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Influenza A virus H1N1 subtype (swine influenza) nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Multiple faecal parasite nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Human parainfluenza virus 3 nucleic acid IVD, kit, nucleic acid technique (NAT)
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024

