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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 167868. The device is manufactured by Safecare Biotech (Hangzhou) Co., 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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In Vitro Diagnostic Device
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Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, rapid ICT, clinical
MHRA Device ID: 167868โ€ขRef: 167868

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

Address

Building 2/203, No.18 Haishu Rd. Cangqian Sub-district, Yuhang District,

Hangzhou, Zhejiang , China

Created Date

Nov 13, 2020

Authorized Representative

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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