Mycoplasma AB Test Cassette: Speedy Semi-Quantitative CRP Evaluation Device
INTRODUCTION
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.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
2.Insufficient specimen volume, incorrect operating procedure or expired tests are the most likely reasons for control band failure.
The Mycoplasma AB Test Cassette's unique, innovative design manifests QL Biotech's commitment towards continuous innovation and advancement in the medical diagnostic field. The CRP Rapid Test Device brought to you by QL Biotech is indeed a tool designed to meet the growing demand for accurate and efficient diagnostic tools in today's fast-paced medical field. This product emphasizes QL Biotech's dedication in developing modern, efficient, and versatile tools vital for an improved diagnostic procedure. The Mycoplasma AB Test Cassette, a CRP semi-quantitative rapid test device indeed encapsulates the company's vision and expertise, emerging as a frontrunner in the biotech industry.