United Kingdom MHRA device registration 165277
Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)
United Kingdom·In Vitro Diagnostic Device·Uniogen Oy·Registered Nov 26, 2024Registration details
- Device ID
- 165277
- MHRA Reference Number
- 165277
- Date Registered
- Nov 26, 2024
- Last Updated
- Apr 5, 2024
Device classification
- Device Type
- In Vitro Diagnostic Device
- Devices
- Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)
- Type
- IVD General
Manufacturer
- Name
- Uniogen Oy
- Address
- Tykistökatu 4 Turku, Finland
- Created Date
- Jan 23, 2023
Authorized Representative
- Relationship Type
- UK Responsible Person
- Address
- Unit 20 Ash Way Thorp Arch Estate Wetherby, England, United KingdomPostcode: LS23 7FA
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About this record
Beta-haemolytic Group B Streptococcus 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 165277. The device is manufactured by Uniogen Oy from Finland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch 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.
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