Finecare Troponin I rapid diagnostic test reagents Troponin I Cardiac Diagnostic Test

Wondfo is a globally recognized fast growing POCT company devoted to R&D, manufacture and sales of rapid diagnostic reagents and medical devices in IVD field. Apart from the Guangzhou headquarters, Wondfo also owns one overseas lab in San Diego, one branch in Chicago and several overseas offices.“Quality is life!” is paramount in everything we do. Wondfo has won good reputation worldwide by providing premium products and professional services. We aim at serving the public, and hence people will trust Wondfo.
1. Quick and easy operation and 99% accuracy.
2. Wondfo has 27 years history, and has won good reputation around the world for good quality products and professional services..
3. Wondfo have got CE certificates, FSC certificates, ISO 9001:2008 and ISO 13485:2012 quality system certification.
4. For in vitro diagnostic use only. For self-testing use only.
The FinecareTM platform provides reliable and quantitative results of various kinds of analytes in human blood or urine within several minutes.
Wondfo CTNI PRINCIPLE
The FinecareTM cTn l Rapid Quantitative Test is based on fluorescence immunoassay technology. The FinecareTM cTn l Rapid Quantitative Test uses a sandwich immunodetection method. When sample is added into the sample well of the Test Cartridge, the fluorescence-labeled detector anti-cTn I antibodies on the sample pad bind to cTn I antigens in blood specimen and they form immune complexes. As the complexes migrate on the nitrocellulose matrix of test strip by capillary action, the complexes of detector antibodies and cTn I are captured to anti-cTn I antibodies that have been immobilized on test strip. Thus the more cTnI antigens in blood specimen, the more complexes accumulated on test strip. Signal intensity of fluorescence of detector antibodies reflect the amount of captured cTnI. TEST PROCEDURE
For complete information and operating procedures, please refer to FinecareTM FIA System Operation Manual. Test shouldbe performed at room temperature.
Before testing, activate “use” in setting then save it. Ensure that the lot number of the Test Cartridge matches ID Chip as well as the Detection Buffer. Insert ID Chip intoFinecareTM FIA System. Step 2: Sampling
Draw 75 μL of whole blood or serum or plasma with a transfer pipette and add into the Detection Buffer tube. Step 3: Mixing
Close the lid of Detection Buffer tube and mix the sample mixture thoroughly by shaking it about 10 times. Step 4: Loading
Pipette 75 μL of sample mixture and load it into the sample well of the Test Cartridge. Step 5: Testing
There are two test modes for FinecareTM FIA System, Standard Test mode and Quick Test mode. Please refer to theOperation Manual of FinecareTM FIA System for details.
a)For Standard Test mode: Insert the Test Cartridge onto the Test Cartridge holder of Finecare™ FIA System right after adding sample mixture to the sample well. Press “Test” to start testing. (Apply to FS-112, FS-113 and FS-205)
b) For Quick Test mode: Set the timer and count down right after adding sample mixtureinto the samplewell and leave it at room temperature for 15 minutes. Then insert the Test Cartridge onto the Test Cartridge holder of Finecare™ FIA System. Press “Test” to start testing. Finecare™ FIA System will start scanning the sample-loaded Test Cartridge immediately. (Apply to FS-112 and FS-113)
Results are displayed on main screen or be printed by press “Print”.
Discard the used Test Cartridge according to local regulations and procedures after released from Finecare™ FIA System.