Advanced CRP/SAA Test Cassette for Semi-Quantitative Rapid Testing (10~30~60 mg/L)
Introducing the cutting-edge CRP/SAA Test Cassette by QL Biotech, specifically designed for semi-quantitative rapid testing with a range of 10~30~60 mg/L. Converging the best of biotech innovation and medical precision, this product presents an accurate and efficient solution to assist healthcare professionals worldwide.
Methodically engineered for professional in vitro diagnostic use, this advanced CRP/SAA Test Cassette is paramount in determining levels of C-reactive Protein (CRP), an inflammation marker often used in diagnostic procedures. The device plays a critical role in advancing diagnostic accuracy and improving patient outcomes. This dependable tool allows healthcare professionals to promptly detect and measure CRP levels, providing crucial insight into a patient's inflammatory status and thereby facilitating more informed therapeutic decisions.
Thanks to the intricate design and superior reliability of the CRP/SAA Test Cassette, it is poised to become an indispensable asset in modern healthcare settings. The device's semi-quantitative capacity allows for a more nuanced understanding of test results, enabling more targeted and refined treatment strategies. It simplifies the diagnostic process without compromising on accuracy, providing practitioners with a swift and reliable determination of CRP levels.
Moreover, QL Biotech is committed to creating diagnostic solutions that not only meet but exceed international standards. With this commitment, we ensure that our CRP/SAA Test Cassette is produced under the strictest quality control measures, bringing professionals the assurance they need to trust the results it delivers. Every CRP/SAA Test Cassette that leaves our facility embodies QL Biotech's dedication to quality, precision, and patient wellbeing. The CRP/SAA Test Cassette by QL Biotech - Redefining rapid diagnostic testing, one result at a time.
PRECAUTIONS
For professional in vitro diagnostic use only.
Do not use after the expiration date indicated on the package. Do not use the test if the foil pouch is damaged. Do not reuse tests.- This kit contains products of animal origin. Certified knowledge of the origin and/or sanitary state of the animals does not completely guarantee the absence of transmissible pathogenic agents. It is therefore recommended that these products be treated as potentially infectious, and handled observing usual safety precautions (e.g., do not ingest or inhale).
- Avoid cross‐contamination of specimens by using a new specimen collection container for each specimen obtained.
- Read the entire procedure carefully prior to any testing.
- Do not eat, drink or smoke in the area where the specimens and kits are handled. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout the procedure and follow standard procedures for proper disposal of specimens. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
- Do not interchange or mix reagents from different lots.
- Humidity and temperature can adversely affect results.
- Used testing materials should be discarded in accordance with local regulations.
INTERPRETATION OF RESULTS
POSITIVE RESULT: Possible Interpretation of CRP Levels
NOTE:
- The intensity of the color in the test region (T) may vary depending on the concentration of analytes present in the specimen. Therefore, any shade of color in the test region should be considered positive. Please note that this is a semi‐quantitative test only, and cannot determine the concentration of analytes in the specimen.
- Insufficient specimen volume, incorrect operating procedure or expired tests are the most likely reasons for control band failure.
INTENDED USE
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The CrP Rapid Test Device (Whole Blood/Serum/Plasma) is used for semi‐quantitative determination and monitoring of CrP concentrations in whole blood/serum/plasma specimens.
C‐reactive Protein (CrP) in patient’s sera has been found in association with acute infections, necrotic conditions and a variety of inflammatory disorders. There is a strong correlation between serum levels of CrP and the onset of the inflammatory process. Monitoring the levels of CrP in
patient’s sera indicates the effectiveness of treatment and the assessment of patient recovery. It is used in particular to differentiate bacterial infections from virus infections.
Moreover, QL Biotech is committed to creating diagnostic solutions that not only meet but exceed international standards. With this commitment, we ensure that our CRP/SAA Test Cassette is produced under the strictest quality control measures, bringing professionals the assurance they need to trust the results it delivers. Every CRP/SAA Test Cassette that leaves our facility embodies QL Biotech's dedication to quality, precision, and patient wellbeing. The CRP/SAA Test Cassette by QL Biotech - Redefining rapid diagnostic testing, one result at a time.