Product Description
Brand Boditech
Sample Type Whole Blood
Pack Size 24T
CAT No SMFP-102
Biomarker Infection
MxA(Myxovirus resistance protein A) is an intracellular blood protein that mediates cellular resistance against a wide range of viruses and elevates in the presence of most acute active viral infections. The level of CRP (C-reactive protein) elevates in the wide status of inflammation and even higher in bacterial infections. The MxA/CRP combo test assists diagnose viral & bacterial infections by measuring virus-specific markers and CRP simultaneously.
Fast and Reliable Infection DifferentiationThe AFIAS MxA/CRP Analyzer delivers simultaneous, quantitative analysis of MxA and CRP markers to help distinguish bacterial from viral infections quickly. Its advanced fluorescent immunoassay technology ensures precise results in just 12 minutes, supporting prompt and informed clinical decisions in both laboratory and point-of-care settings.
Effortless Operation and Data HandlingEngineered for user convenience, this analyzer features fully automatic operation and factory calibration, eliminating manual setup. Integrated barcode scanning and versatile USB/LAN connectivity streamline data management, while the built-in thermal printer ensures thorough and immediate documentation-key for busy clinical workflows.
Compact, Portable, and SafeWith its lightweight, portable design and low-noise operation, the AFIAS MxA/CRP Diagnosis Analyzer fits effortlessly into varied clinical environments. Safety is prioritized: there's no direct sample contact needed. Durable plastic and electronic materials ensure long-term reliability, and its high-contrast LCD display enables clear result interpretation every time.
FAQ's of Boditech AFIAS MxA/CRP:
Q: How is the Boditech AFIAS MxA/CRP analyzer used in clinical settings?
A: The analyzer is used for quantitative measurement of MxA and CRP levels via whole blood, serum, or plasma samples. This provides critical data to help distinguish bacterial from viral infections, supporting more targeted treatment decisions in laboratories and point-of-care environments.
Q: What is the process for running a test with this analyzer?
A: Simply collect 100 L of the patient's sample (whole blood, serum, or plasma), load it into the test cartridge, and insert it into the analyzer. The device automatically measures MxA and CRP, outputs results in 12 minutes, and logs data via its built-in printer and connectivity options.
Q: When should I use the AFIAS MxA/CRP analyzer for patient evaluation?
A: Use the analyzer when rapid differentiation between bacterial and viral infections is needed, such as for patients presenting with fever or other infection symptoms where immediate treatment decisions are essential.
Q: Where can the AFIAS MxA/CRP analyzer be installed and operated?
A: The compact design and portability allow it to be placed in laboratories, clinic examination rooms, or other point-of-care environments, provided ambient temperature ranges between 15 and 32C and there is access to an AC power source.
Q: What benefits does the integrated barcode scanner and data management system provide?
A: The barcode scanner simplifies sample identification and tracking, reducing manual errors, while USB and LAN connectivity enable easy data export, storage, and patient record integration, enhancing workflow efficiency and data accuracy.
Q: How safe is it to operate the analyzer and handle samples?
A: The AFIAS MxA/CRP is designed with operator safety in mind; there is no need for direct contact with samples, minimizing exposure risk. The automatic operation further enhances user safety and convenience.
Q: What maintenance or calibration is required for optimal performance?
A: The analyzer is factory calibrated, so no routine user calibration is necessary. Basic care, such as storage in a cool, dry place, will help ensure long-term reliability and high accuracy.