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5 Pack - Fentanyl Instant Urine Drug Test Kit - 200 ng/mL

5 Pack - Fentanyl Instant Urine Drug Test Kit - 200 ng/mL

$ 3.69

Availability: 100 in stock
  • All returns accepted: Returns Accepted
  • Condition: New
  • Labels & Certifications: FDA 510K Compliant
  • Manufacturer Warranty: None
  • Refund will be given as: Money back or replacement (buyer's choice)
  • Return shipping will be paid by: Seller
  • Drug Type: Fentanyl
  • Restocking Fee: No
  • Product Line: Dip Card
  • Brand: One Step
  • Sample Type: Urine
  • Type: Home Drug Test
  • Country/Region of Manufacture: China
  • MPN: HDFTY-114
  • Expiration Date: 3-2022
  • Item must be returned within: 30 Days

    Description

    5 individually wrapped tests
    Urine Drug Test for Fentanyl Detection
    Product Description:
    An affordable workplace test to determine if employees are using opiods products
    Easy-to-use test kit generating accurate results in minutes
    Instructions
    :
    Have donor provide urine sample and let stand until it's room temperature. Open the foil pouch and remove the test device.
    Remove the cap from the test device
    Immerse the absorbent tip into the urine sample for 10-15 seconds. Urine sample should not touch the plastic device
    Replace the cap over the absorbent tip and lay the device flatly on a non-absorptive clean surface
    Read results in 5 minutes (do not interpret results after 10 minutes
    Drug cut-off
    :
    FEN: Fentanyl - cut-off 200 ng/mL
    Results
    :
    Positive:
    One colored line appears in the control (C) region & no line appears in the test region (T).
    Negative:
    One colored line appears in the control (C) region, and another colored line in the test (T) region. The color intensity of the test line may be weaker or stronger than that of the control line, but regardless of the intensity, the result is negative.
    Invalid:
    No line appears in the control zone “C”. If the test device does not produce a band in the control region, check the testing procedures, samples, and/or control materials and repeat the test using a new device.