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Finecare™ Troponin Control – Cardiac cTnI Quality Control for Rapid Tests & FIA Analyzers

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The Finecare™ Troponin Control Set is a multi-level quality control (QC) product designed to ensure the accuracy and reliability of cardiac troponin I (cTnI) assays used in Finecare rapid tests and Finecare FIA analyzers. Quality control materials play a crucial role in daily laboratory QC procedures, external quality assessment, and validation of new reagent lots.

This control set helps verify that Finecare cTnI test systems (including rapid tests and immunofluorescence analyzers) are functioning correctly, producing consistent results, and meeting performance expectations as defined by clinical and laboratory standards.

Intended for in-vitro diagnostic (IVD) use only, the Finecare Troponin Control Set supports clinical laboratories, emergency departments, and point-of-care testing sites in maintaining high standards of cardiac biomarker testing.

 Pack Size & Kit Contents

Typical Pack Configuration

  • Level 1 (Normal/Low) Control

  • Level 2 (High) Control

  • Instructions for Use (IFU)

  • Stability and Target Value Chart

Note: Some kits may include additional vials or greater volumes depending on manufacturer packaging.

 Key Features & Benefits

✔ Designed specifically for Finecare cTnI assays

✔ Provides Level 1 & Level 2 controls representing expected clinical ranges

✔ Ensures daily QC verification and accuracy monitoring

✔ Helps detect reagent, instrument, or operator issues

✔ Supports compliance with laboratory standards

✔ Stable and easy to handle

✔ For in-vitro diagnostic use only

 Purpose of Troponin Controls

Quality controls are used to:

  • Validate assay performance daily

  • Confirm reader/POCT analyzer accuracy

  • Ensure lot-to-lot consistency

  • Detect instrument malfunction or drift

  • Support lab accreditation requirements

Control Levels & Interpretation

Control LevelTypical RangeClinical Context
Level 1 (Normal/Low)Within normal or near-normal cTnI rangeConfirms baseline assay accuracy
Level 2 (High)Elevated cTnI levelsVerifies detection capability near clinical decision thresholds


Usage Instructions 

  1. Bring control vials to room temperature

  2. Mix gently before use

  3. Process each control sample like a patient specimen

  4. Run on Finecare rapid test or Finecare FIA reader

  5. Compare results to manufacturer-provided ranges

  6. Document results in QC log


10,500.00 KSh 10,500.00 KSh

  • Packaging
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