AMP快速檢測卡

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One StepAmphetamine Test Device

A rapid, one step test for the qualitative detection of Amphetamines in human urine.

For healthcare professionals including  professionals at point of care sites

For professional in vitro diagnostic use only.

The urine specimen must be collected in a clean and dry container. Urine collected at any time of the day may be used. Urine specimens exhibiting visible particles should be centrifuged, filtered, or allowed to settle to obtain clear specimen for testing.

Specimen Storage

Urine specimens may be stored at 2-8°C for up to 48 hours prior to assay. For long-term storage, specimens may be frozen and stored below -20°C. Frozen specimens should be thawed and mixed before testing.

Allow the test device, urine specimen, and/or controls to reach room temperature (15-30oC) prior to testing.

1.     Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.

2.     Place the test device on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 100ml) to the specimen well (S) of the test device, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below.

3.     Wait for the colored line(s) to appear. The result should be read at 5 minutes.  Do not interpret the result after 10 minutes.

INTERPRETATION OF RESULTS

(Please refer to the illustration above)

NEGATIVE:* Two lines appear. One colored line should be in the control region (C), and another apparent colored line should be in the test region (T). This negative result indicates that the Amphetamine concentration is below the detectable level (1,000 ng/mL).

* NOTE: The shade of color in the test line region (T) will vary, but it should always be considered as negative whenever there is even a faint line.

POSITIVE: One colored line appears in the control region (C). No line appears in the test region (T). This positive result indicates that the Amphetamine concentration exceeds the detectable level (1,000 ng/mL).

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test device. If the problem persists, discontinue using the lot immediay and contact your local distributor.

 掃一掃二維碼：

【公司名稱】 廣州健侖生物科技有限公司

【市場部】       楊永漢
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【騰訊 】
【公司地址】 廣州市清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號二期2幢101-103室