United Kingdom MHRA device registration 89103

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

United Kingdom·In Vitro Diagnostic Device·ReLIA Biotechnologies (Jiangsu), Inc.·Registered Nov 26, 2024

Registration details

Device ID: 89103
MHRA Reference Number: 89103
Date Registered: Nov 26, 2024
Last Updated: Apr 29, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: SARS-CoV-2 neutralizing antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

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

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About this record

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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