SARS-CoV-2 total antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

SARS-CoV-2 total 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 132320. The device is manufactured by Promega Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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SARS-CoV-2 total antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 132320•Ref: 132320

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2 total antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 10, 2024

Last Updated

Oct 10, 2023

Manufacturer Information

Name

Promega Corporation

Address

2800 Woods Hollow Road

Madison, WI, United States

Created Date

Jan 14, 2022

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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SARS-CoV-2 total antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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