United Kingdom MHRA device registration 68709

Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Shenzhen JetMay Care Limited·Registered Nov 26, 2024

Registration details

Device ID: 68709
MHRA Reference Number: 68709
Date Registered: Nov 26, 2024
Last Updated: Apr 16, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Shenzhen JetMay Care Limited
Address: District 02, 1F & 3F, Block A, Haikexing Sinovac Strategic Emerging Industrial Park Pingshan District
Shenzhen, Guangdong, China
Created Date: Jul 30, 2020

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

Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68709. The device is manufactured by Shenzhen JetMay Care Limited from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang Ltd.

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