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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.

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In Vitro Diagnostic Device
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Amniotic fluid leak detection device IVD
MHRA Device ID: 98082โ€ขRef: 98082

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

Manufacturer Information

Address

747 West 4170 South

Murray, Utah, United States

Created Date

Aug 24, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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