PreKNOW Urine Single Drug Dip Card

PreKnow Single Urine Drug Test Dip Card (CLIA Waived)

15T 01

standard box

15T 01

1/2

One step
FDA approved and CLIA waived
24 months shelf life
Perfect for self testing at home and office
Easy to read results
Results within 5 minutes

Model

Test Item

Test per Box

P-TH501

P-CO501

P-BA501

P-MO501

P-OP501

P-AM501

P-MD501

THC 50ng/mL

COC 300ng/mL

BAR 300ng/mL

MOP 300ng/mL

OPI 2000ng/mL

AMP 1000ng/mL

MDMA 500ng/mL

25 tests

* For label design and mold design, please be free to contact us.

Specifications

PreKnow® Single Urine Drug Test Dip Card is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at a cut-off concentration.

The product is FDA approved, CLIA-Waived and CE marked, It is ideal for use in workplace screening, forensics, emergencies, detoxification treatment, addiction management treatment, transport authorities and custom and home use.

How to use

Test must be in room temperature (50.0℉ ~86.0℉/10 ºC ~30 ºC)

Open the sealed pouch by tearing along the notch. Remove the test device from the pouch.
Hold the one side of the device with one hand. Use the other hand to pull out the cap and expose the absorbent end.
Immerse the absorbent end into the urine sample about 10 seconds. Make sure that the urine level is not above the “arrow” marker printed on the front of the device.
Lay the device flat on a clean, dry, non-absorbent surface.
Read the result at 5 minutes. Do not read after 5 minutes.

Read the result

Positive (+)

One colored line appears in the control line region (C). No line appears in the test line region (T). This positive result indicates that the drug concentration exceeds the detectable level.

Negative (-)

Two lines appear. One colored line should be in the control line region (C), and another apparent colored line should be in the test line region (T). This negative result indicates that the drug concentration is below the detectable level.

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. If the problem persists, discontinue using the lot immediately and contact your local distributor with the lot number.