General specimen collection kit IVD, home-use
United Kingdom·In Vitro Diagnostic Device·Zymo Research Corporation·Registered Nov 22, 2024- Device ID
- 186982
- MHRA Reference Number
- 186982
- Date Registered
- Nov 22, 2024
- Last Updated
- May 4, 2024
- Device Type
- In Vitro Diagnostic Device
- Devices
- General specimen collection kit IVD, home-use
- Type
- Class A
- Address
- 17062 Murphy Avenue Irvine, CA, United States
- Created Date
- Feb 14, 2024
- Name
- CASUS UKRP LTD
- Relationship Type
- UK Responsible Person
- Address
- 107-111 Fleet Street London, England, United KingdomPostcode: EC4A 2AB
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by CASUS UKRP LTD in the UK
General 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 186982. The device is manufactured by Zymo Research Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CASUS UKRP 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.