CK-MB Fast Test Kit (Immunofluorescence Assay)

Primary DI

06954414702156

Basic UDI-DI Code

B-06954414702156

Reference

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Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

Getein Biotech, Inc.

CK-MB Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of CK-MB in serum, plasma or whole blood. This test is used as an aid in the clinical diagnosis, prognosis and evaluation of myocardial injury such as Acute Myocardial Infarction (AMI), Unstable Angina, Acute Myocarditis and Acute Coronary Syndrome (ACS). For professional and laboratory use only.

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).