Finecare™ CK-MB Rapid Test – Cardiac Creatine Kinase-MB Rapid Diagnostic Kit | Acute Myocardial Infarction Marker

The Finecare™ CK-MB Rapid Test is a qualitative immunofluorescence assay for the detection of Creatine Kinase-MB (CK-MB) in whole blood, serum, or plasma. CK-MB is a cardiac biomarker released into the bloodstream after cardiac muscle injury, especially in acute myocardial infarction (AMI).

Designed to be used with the Finecare™ FIA fluorescence immunoassay reader, this rapid test delivers precise, objective results within minutes, making it ideal for emergency departments, urgent care, cardiac care units, and point-of-care (POC) settings.

This assay enhances early detection of cardiac events, supports triage decisions, and complements other cardiac markers such as cTnI and Myoglobin.

 Pack Size & Kit Contents

Pack Size Options:

• 25 Tests/Box

Each Kit Contains:

• CK-MB test cartridges/strips

• Buffer reagent

• Disposable sample applicators

• Instructions for Use (IFU)

Compatibility:

✔ Finecare™ FIA Reader (e.g., FIA-100 or compatible model)

 Key Features & Benefits

✔ Detects Creatine Kinase-MB (CK-MB) – a marker of cardiac muscle damage

✔ Rapid results (typically within 10-15 minutes)

✔ Works with whole blood, serum, or plasma

✔ Uses Finecare fluorescence immunoassay technology

✔ Enhances early AMI diagnosis alongside cTnI and Myoglobin

✔ Compact and easy-to-use at the point-of-care

✔ Minimal training required

✔ For in-vitro diagnostic use only

Clinical Applications

• Suspected Acute Myocardial Infarction (AMI)

• Cardiac injury screening

• Triage of chest pain in emergency settings

• Monitoring cardiac biomarker trends along with cTnI/Myoglobin

• Secondary confirmation in cardiac events

Sample Requirements

✔ Whole blood (capillary or venous)

✔ Serum

✔ Plasma

Refer to the IFU for exact volume and handling instructions.

 Result Interpretation

Note: Always interpret CK-MB in context with ECG, clinical symptoms, and other biomarkers (cTnI, Myoglobin).

 Usage Instructions 

1. Collect the sample (whole blood/serum/plasma)

2. Apply to the Finecare™ CK-MB test cartridge

3. Insert into the Finecare FIA Reader

4. Await digital results

5. Record & interpret according to clinical guidelines

   (Exact volumes and timing are in the IFU.)