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Complement reagent IVD - UK MHRA Medical Device Registration

Complement reagent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92333. The device is manufactured by Immucor GTI Diagnostics, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting 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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Complement reagent IVD
MHRA Device ID: 92333โ€ขRef: 92333

Device Type

In Vitro Diagnostic Device

Devices

Complement reagent IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Address

20925 Crossroad Circle

Waukesha, Wisconsin, United States

Created Date

Aug 4, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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