United Kingdom MHRA device registration 125102

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

United Kingdom·In Vitro Diagnostic Device·Princeton BioMeditech Corporation·Registered Nov 26, 2024

Registration details

Device ID: 125102
MHRA Reference Number: 125102
Date Registered: Nov 26, 2024
Last Updated: Sep 28, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

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

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About this record

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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