Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 125102. The device is manufactured by Princeton BioMeditech Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 125102•Ref: 125102

Device Type

In Vitro Diagnostic Device

Devices

Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Sep 28, 2024

Manufacturer Information

Name

Princeton BioMeditech Corporation

Address

4242 US Highway 1

Monmouth Junction, New Jersey, United States

Created Date

Dec 21, 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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Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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