Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80820. 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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Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical

MHRA Device ID: 80820•Ref: 80820

Device Type

In Vitro Diagnostic Device

Devices

Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

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

DJ Fang

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Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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