Verify® Menopause Self Test
In stock
Verify® Menopause Self Test
【 REAGENTS 】
The test contains anti-FSH and anti-FSH particles coated on the membrane.
【 PRECAUTIONS 】
Please read all the information in this leaflet before performing the test.
Do not use after the expiration date.
The test must remain in the sealed pouch until use.
Store in a dry place at 2-30°C (36-86°F). DO NOT FREEZE.
Do not use if case is torn or damaged.
Keep out of reach of children.
For in vitro diagnostic use only .
Do not open the foil test pouch until you are ready to begin testing.
Use the test only once.
The used test must be disposed of according to local regulations.
【 STORAGE AND STABILITY 】
Store in the pouch at room temperature or refrigerated (2-30°C). The test is stable until the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.
【 SAMPLE COLLECTION AND PREPARATION 】
The urine sample should be collected in a clean, dry container. A first morning urine sample is preferable, as it generally contains the highest concentration of FSH; however, urine samples collected at any time of day can be used. Urine samples with visible precipitates should be centrifuged, filtered, or allowed to settle to obtain a clear sample for analysis.
【 SAMPLE STORAGE 】
Urine samples can be stored at 2-8°C for up to 48 hours before testing. For extended storage, samples can be frozen and stored below -20°C. Frozen samples must be thawed and mixed before testing. 【 MATERIALS PROVIDED 】
Midstream Test
【 MATERIALS REQUIRED BUT NOT PROVIDED 】
Timer
【 INSTRUCTIONS 】
WHEN TO START THE TEST
In the presence of monthly menstrual cycles, perform the first test during the first week of the cycle (days 2-7, considering day 1 as the first
(day of menstruation). If the result is negative but symptoms persist, repeat with a second test a week later.
If you no longer have regular periods, take the test at any time during the month and repeat with a second test 1 week later.
【 HOW TO USE 】
Before performing the test, allow the urine specimen and/or controls to reach room temperature (15-30°C). 1. Determine the day to begin testing. (See previous section: "WHEN TO START TESTING").
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Bring the pouch to room temperature before opening. Remove the test from the sealed pouch and use it within one hour.
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Remove the midstream cap, place the absorbent tip into the urine stream or immerse the absorbent tip (≥2/3) in the urine of a
clean container for at least 10-15 seconds.
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Replace the cap on the test, then place the midstream on a clean, stable surface, with the inspection window facing up, and start
the timer immediately.
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When the test begins the detection process, you may notice a light colored stream moving through the control window. Read
the result after 3 minutes . Do not interpret the result after 10 minutes.
【 READING THE RESULTS 】
POSITIVE: Two lines are visible and the line in the test region (T) is equal to or darker than the line in the control region (C). A positive result
This means your FSH level is higher than normal. Record your results and compare them to the graph above for interpretation .
NEGATIVE: Two lines are visible, but the line in the test area (T) is fainter than the line in the control area (C), or no line appears in the test area (T). A negative result means that your FSH level is not currently elevated. Record your results and compare them to the graph above for interpretation .
INVALID: The control line is not displayed. The most likely reasons for the control line not being displayed are This error may be due to insufficient sample volume or incorrect procedural techniques. Review the procedure and repeat the analysis with a new test. If the problem persists, discontinue use of the test kit immediately and contact your local distributor.
TEST INTERPRETATION
For women experiencing premenopausal symptoms along with irregular menstrual cycles.
【 INSPECTION PROCEDURE 】
A procedural control is included in the test. The colored line appearing in the control region (C) is considered an internal procedural control. It confirms sufficient sample volume, adequate membrane absorption, and correct procedural technique.
【 LIMITATIONS 】
There is a possibility that this test may produce false positive or false negative results. Consult your doctor before making any medical decisions. Invalid results are most likely caused by not following the instructions correctly. Review the instructions and repeat the test with a new test. If the problem persists, stop using the test kit immediately and contact your local distributor.
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