Finecare™ hs-CRP Rapid Test – High-Sensitivity C-Reactive Protein | 25 Tests/Box

The Finecare™ hs-CRP Rapid Test is a qualitative/semiquantitative immunofluorescence assay for the high-sensitivity detection of C-Reactive Protein (CRP) in human whole blood, serum, or plasma. High-sensitivity CRP (hs-CRP) is a key inflammation biomarker routinely used in assessing cardiovascular risk, chronic inflammation, and response to therapy.

Designed for use with the Finecare™ FIA (fluorescence immunoassay) reader, this rapid test delivers objective digital results within minutes, enabling healthcare providers to make faster decisions in cardiac risk evaluation, primary care, and point-of-care settings.

 Pack Size & Kit Contents

Pack Size: 25 Tests per Box

Each Kit Contains:

• 25 × hs-CRP rapid test cartridges/strips

• Buffer reagents

• Disposable sample applicators

• Instructions for Use (IFU)

Compatibility:

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

Key Features & Benefits

✔ Detects high-sensitivity C-Reactive Protein (hs-CRP)

✔ Rapid results (typically within 10–15 minutes)

✔ Works with whole blood, serum, or plasma

✔ Uses Finecare fluorescence immunoassay technology

✔ Objective digital results on Finecare reader

✔ Minimal training required

✔ Useful in cardiovascular risk assessment and inflammation monitoring

✔ For in-vitro diagnostic use only

 Clinical Applications

• Cardiovascular risk stratification

• Detection of chronic low-grade inflammation

• Monitoring anti-inflammatory therapy

• Point-of-care assessment in primary care clinics

• Triage in emergency settings

 Sample Requirements

✔ Whole blood (capillary or venous)

✔ Serum

✔ Plasma

(Refer to IFU for exact volumes.)

hs-CRP Result Interpretation

Note: These ranges are standard general guidance; always correlate with clinical context and patient history.

 Usage Instructions 

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

2. Apply sample to the test cartridge

3. Insert into the Finecare FIA Reader

4. Wait for automated digital readout

5. Interpret per clinical reference ranges

   (Exact procedures and times are in the IFU.)