Amniotic fluid leak detection device IVD - UK MHRA Medical Device Registration
Amniotic fluid leak detection device IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98082. The device is manufactured by Clinical Innovations, LLC. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, 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
Amniotic fluid leak detection device IVD
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Address
747 West 4170 South
Murray, Utah, United States
Created Date
Aug 24, 2021
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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