TEST PROCEDURE:

1. Bring the pouched test device to room temperature (15-30℃) prior to testing. Do not open the pouch until ready to perform the assay.
2. Remove the test device from the sealed pouch. Lay it on a flat, clean and dry surface.
3. For serum or plasma specimens, hold the dropper vertically, transfer 2 drops of serum or plasma (approximately 50 µL) to the sample well (S) of the test device and start the timer.
4. Read the result between 5-10 minutes. Do not interpret results after 20 minutes.

INTERPRETATION OF RESULTS:

Positive:
Two pink-colored lines appear in the result window, one in the control region "C" and another one in the test region "T". This indicates a positive result and the AFP having been detected.
Negative:
Only the control line appears in the result window. This indicates a negative result and no AFP having been detected.
Invalid:
If no line appears in the control region, the test result is invalid regardless of the presence or absence of the test line.
NOTE:
Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for the control line failure. Review the procedure and repeat the test with a new device. If problem persists, please contact your local distributor.

Description	Specimen	Format	Catalog No.	Sensitivity	Package Size	Strip Width	Certificate
(AFP) Alpha-Fetoprotein Test	Serum/Plasma	Strip	E10-11	20ng/mL	50 Tests	3.0 mm	CE
		Cassette	E10-20		25 Tests	4.0 mm
	Whole Blood		E10-21		25 Tests	4.0 mm