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

SARS-CoV-2 neutralizing 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 89103. The device is manufactured by ReLIA Biotechnologies (Jiangsu), Inc. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is KINGSMEAD SERVICE LIMITED.

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

MHRA Device ID: 89103•Ref: 89103

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Apr 29, 2024

Manufacturer Information

Name

ReLIA Biotechnologies (Jiangsu), Inc.

Address

G30, North of Xinyang Road, East of Koutai Road, CMC

Taizhou, China

Created Date

Jul 15, 2021

Authorized Representative

Name

KINGSMEAD SERVICE LIMITED

Relationship Type

UK Responsible Person

Address

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London, England, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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

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