Interferon gamma release IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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

MHRA Device ID: 140515•Ref: 140515

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 17, 2023

Manufacturer Information

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

DJ Fang

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Interferon gamma release IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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