HLA class I antibody screening IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

HLA class I antibody screening IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92338. 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.

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HLA class I antibody screening IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 92338•Ref: 92338

Device Type

In Vitro Diagnostic Device

Devices

HLA class I antibody screening IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Name

Immucor GTI Diagnostics, Inc.

Address

20925 Crossroad Circle

Waukesha, Wisconsin, United States

Created Date

Aug 4, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

DJ Fang

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HLA class I antibody screening IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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