United Kingdom MHRA device registration 140515

Interferon gamma release IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·Hainan VTI Clinical Immunology Lab Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 140515
MHRA Reference Number: 140515
Date Registered: Nov 26, 2024
Last Updated: Oct 17, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Interferon gamma release IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: Hainan VTI Clinical Immunology Lab Ltd.
Address: No.273 Nanhai Avenue, Xiu Ying District,
Haikou, Hainan, China
Created Date: Mar 18, 2022

Authorized Representative

Name: Wellkang Ltd
Relationship Type: Authorised Representative (Northern Ireland)
Address: Enterprise Hub, NW Business Complex 1 Beraghmore Road
Derry, Northern Ireland, Northern Ireland, United Kingdom
Postcode: BT48 8SE

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About this record

Interferon gamma release IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 140515. The device is manufactured by Hainan VTI Clinical Immunology Lab Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang Ltd.

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