Coagulation Quality Control

To achieve optimal assay performance in coagulation testing, it is crucial to select the appropriate coagulation quality control. UD-Bio offers an array of quality control options for APTT, PT, TT, and FIB (Fbg) analysis, which can be seamlessly used with most coagulation testing instruments. Our coagulation quality control solutions aid in streamlining the quality control workflow, enhancing reliability, and minimizing the potential for inaccurate patient test results. By utilizing our comprehensive quality control products, laboratories can ensure the accuracy and precision of their coagulation assays, ultimately improving patient care.

Principle：

The Coagulation Quality Control Products are created by meticulously processing the sodium citrate anticoagulant plasma from humans to simulate typical plasma samples used during coagulation analyses. These products are utilized in detecting coagulation disorders such as APTT, PT TT, and FIB (Fbg) and the results should fall within the reference range. The manufacturing process ensures that the final product meets the necessary standards for accurate and reliable coagulation testing. Users of these products are guaranteed consistent and precise results every time.

Performance Characteristics：

The reference range for activation of partial thromboplastin time (APTT) should be observed for normal results.

Maintaining a prothrombin time (PT) within the reference interval is crucial.

It is important for the thrombin time (TT) to fall within the reference range.

Normal levels of fibrinogen, also known as FIB, fall within the reference range.

5. Intra-vial Deviation: CV≤5%;

To ensure safety and prevent transmission of infectious diseases, it is important that individuals undergoing certain medical procedures have negative results for HBsAg, HCV antibody, HIV-1/2 antibody, and syphilis. These tests help to identify potential infections and minimize the risk of spreading these diseases to others. Therefore, it is essential to undergo these tests and obtain negative results before undergoing medical treatments or procedures. This is a crucial step in safeguarding both the patient and healthcare providers.

Storage and Stability：

1. 2℃ ~ 8℃ storage period for 2 years;

The expiry date of the opened vial once it is dissolved is 6 months, and it should be stored at a temperature of 2~8 ℃. Please ensure that you follow these instructions to maintain the validity of the medication.

hours.

Specification:

1.0ml x1 bottle

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