Product Description
Brand Acon
Sample Type Serum/ Plasma
Pack Size 25T
CAT No F131-90111
Biomarker Anemia
The Vitamin D FIA Test is a fluorescence immunoassay for the quantitative determination of total 25(OH) VD in human serum/plasma. It is intended as an aid in the assessment of vitamin D sufficiency.
Fast and Accurate Vitamin D QuantificationThe Acon FIAflex Vitamin D FIA Test delivers precise results in under 15 minutes, enabling timely assessment of Vitamin D levels in patient samples. Utilizing advanced fluorescence immunoassay technology, the kit ensures high sensitivity and accuracy (>95%) for effective diagnosis and monitoring. Its automated operation and digital result display streamline workflow and reduce human error, making it ideal for busy clinical laboratories.
User-Friendly Design and Simple OperationDesigned for healthcare professionals, the test kit provides seamless usability with minimal hands-on time. The system's automatic process, clear instructions, and intuitive cartridge loading make it straightforward to operate, even in high-throughput settings. Factory calibration and internal controls further guarantee consistent performance across each test run.
Reliability and Flexible Data ManagementThe FIAflex test supports secure sample and lot tracking, facilitated by included internal controls and digital data export options (USB/RS232). With durable packaging and a shelf life of 18 months, the test is built for clinical environments. Storage and usage conditions are flexible, ensuring dependable functionality across various laboratory settings.
FAQ's of Acon FIAflex Vitamin D FIA Test:
Q: How can the Acon FIAflex Vitamin D FIA Test be used for clinical Vitamin D detection?
A: Healthcare professionals use the Acon FIAflex Vitamin D FIA Test for in-vitro quantitative detection of Vitamin D in human serum or plasma. The test involves loading a patient sample into the provided test cartridge, inserting it into a compatible FIAflex analyzer, and receiving results within 15 minutes, thanks to automated processing and digital interpretation.
Q: What sample types are suitable for this Vitamin D FIA test, and how is accuracy ensured?
A: This test is validated for use with human serum or plasma samples. High accuracy (greater than 95%) is maintained through factory calibration and built-in internal controls in every kit, ensuring consistent, reliable results across different test lots.
Q: When should laboratories choose this immunoassay over other Vitamin D detection methods?
A: Laboratories benefit from the FIAflex test's rapid turnaround and reliability when timely and precise Vitamin D quantification is needed, for example, in patient screening or after supplementation. Its rapid result time and automated process reduce waiting and procedural errors, especially in busy clinical settings.
Q: Where should the FIAflex Vitamin D test kits be stored, and what are the recommended operating conditions?
A: Store the FIAflex test kit in a controlled environment between 2C and 30C, away from direct sunlight. For accurate operation, maintain an ambient testing temperature of 15-30C. These conditions help preserve reagent integrity and the performance of internal controls.
Q: What is the process for interpreting and exporting test results?
A: Results are automatically interpreted by the connected FIAflex analyzer and displayed digitally, minimizing the risk of subjective error. Test data can be easily exported via USB or RS232 interfaces for recordkeeping or integration with laboratory information systems.
Q: Who is intended to use the Acon FIAflex Vitamin D FIA Test, and what are the main benefits?
A: This test kit is intended for trained healthcare professionals in clinical laboratories. The main benefits include rapid and highly accurate quantification of Vitamin D, easy operation, robust internal controls, and reliable traceability via lot number tracking.