Faecal specimen collection kit IVD, home-use
United Kingdom·In Vitro Diagnostic Device·GP Medical Devices A/S·Registered Nov 26, 2024- Device ID
- 169731
- MHRA Reference Number
- 169731
- Date Registered
- Nov 26, 2024
- Last Updated
- Apr 16, 2024
- Device Type
- In Vitro Diagnostic Device
- Devices
- Faecal specimen collection kit IVD, home-use
- Type
- Class A
- Address
- Nupark 51 Holstebro, Denmark
- Created Date
- Mar 30, 2023
- Relationship Type
- UK Responsible Person
- Address
- Office 32 19-21 Crawford Street London, United KingdomPostcode: W1H 1PJ
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by CMC Medical Devices LTD in the UK
Faecal specimen collection kit IVD, home-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169731. The device is manufactured by GP Medical Devices A/S from Denmark, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices 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.