Faecal specimen container IVD, transport buffer/medium - UK MHRA Medical Device Registration
Faecal specimen container IVD, transport buffer/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 186983. 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.
Device Type
In Vitro Diagnostic Device
Devices
Faecal specimen container IVD, transport buffer/medium
Type
Class A
Date Registered
Nov 22, 2024
Last Updated
May 4, 2024
Address
17062 Murphy Avenue
Irvine, CA, United States
Created Date
Feb 14, 2024
Name
CASUS UKRP LTDRelationship Type
Address
107-111 Fleet Street
London, England, United Kingdom
Postcode: EC4A 2AB
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