Creatine kinase myocardial isoenzyme (CKMB) IVD, control - UK MHRA Medical Device Registration

Creatine kinase myocardial isoenzyme (CKMB) IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204902. The device is manufactured by Accucise Diagnostics Inc. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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Creatine kinase myocardial isoenzyme (CKMB) IVD, control

MHRA Device ID: 204902•Ref: 204902

Device Type

In Vitro Diagnostic Device

Devices

Creatine kinase myocardial isoenzyme (CKMB) IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 14, 2024

Manufacturer Information

Name

Accucise Diagnostics Inc.

Address

Suite 501&601, Building 9, Medpark, 188 Fuchunjiang Rd., SND

Suzhou Province, China

Created Date

Nov 8, 2024

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from Accucise Diagnostics Inc. (10)

Other Products from Same Authorized Representative (10)

Creatine kinase myocardial isoenzyme (CKMB) IVD, control - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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