Accutest 10 Panel Drug Dip Test – 25/Box (COC / AMP / MET / THC / MTD / OPI / PCP / BAR / BZO / MDMA)

$180.00

FDA 510(k) Cleared
CLIA Moderate Complexity
Professional Use

25 tests per box$7.20 per test

The Accutest 10 Panel Drug Dip Test is a one-step urine screening card for the simultaneous, qualitative detection of AMP, BAR, BZO, COC, MDMA, MET, MTD, OPI, PCP and THC. Read results at five minutes.

  • Screens 10 drugs and drug metabolites in human urine
  • Simple dip-card format with no instrument required
  • Built-in procedural controls
  • No additional reagents required
  • 25 individually packaged tests per box
Quantity Discounts
1-5 6-10 11+
$180.00 $165.60 $156.60

Accutest 10 Panel Drug Dip Test Overview

The Accutest 10 Panel Drug Dip Test, reference DS130AC425, is a lateral-flow chromatographic immunoassay for the simultaneous, qualitative detection of 10 drugs and drug metabolites in human urine. This professional dip-card configuration screens for amphetamine, barbiturates, benzodiazepines, cocaine metabolite, MDMA, methamphetamine, methadone, opiates, phencyclidine and marijuana metabolite.

FDA 510(k) Cleared
10-Panel Screening
Results at 5 Minutes
25 Tests per Box

Features and Benefits

Ten-drug configuration
Screens AMP, BAR, BZO, COC, MDMA, MET, MTD, OPI, PCP and THC simultaneously.

Fast results
Drug-screen results should be read at five minutes.

Simple dip-card format
Immerse the exposed test strips directly into a collected urine specimen.

No instrument required
Results are interpreted visually without a separate reader or analyzer.

Built-in procedural controls
Control lines help verify sufficient specimen volume, membrane wicking and proper test procedure.

Evaluated performance
Performance varies by analyte and comparison method; refer to the package insert for the complete study data.

Product Details

Reference
DS130AC425
SKU
DTK-109101

Brand Accutest
Manufacturer Jant Pharmacal Corporation
Test format 10-panel urine drug-screen dip card
Specimen Human urine
Test method Lateral-flow chromatographic immunoassay
Result time Read at 5 minutes
Regulatory status FDA 510(k) cleared; CLIA moderate complexity; professional use
Adulteration testing Not included in this configuration
Package size 25 tests per box
Storage Store in the sealed pouch at 36–86°F (2–30°C); do not freeze
Shelf life Stable through the expiration date printed on the sealed pouch

Detectable Drugs and Cutoffs

Detected analyte Abbreviation Calibrator Cutoff
Amphetamine AMP d-Amphetamine 1,000 ng/mL
Barbiturates BAR Secobarbital 300 ng/mL
Benzodiazepines BZO Oxazepam 300 ng/mL
Cocaine metabolite COC Benzoylecgonine 300 ng/mL
Ecstasy MDMA d,l-Methylenedioxymethamphetamine 500 ng/mL
Methamphetamine MET d-Methamphetamine 1,000 ng/mL
Methadone MTD Methadone 300 ng/mL
Opiates OPI Morphine 2,000 ng/mL
Phencyclidine PCP Phencyclidine 25 ng/mL
Marijuana metabolite THC 11-nor-Δ9-THC-9-COOH 50 ng/mL

Cutoffs indicate the concentrations used by the screening assay. They do not indicate the amount of a drug consumed, when it was consumed or the degree of impairment.

How to Perform the Test

  1. Allow the test card, urine specimen and controls, if used, to reach room temperature between 59–86°F (15–30°C).
  2. Remove the test card from its sealed pouch and use it promptly.
  3. Remove the cap from the end of the test card.
  4. With the arrows pointing toward the urine specimen, immerse the exposed strips vertically in the specimen for at least 10–15 seconds.
  5. Immerse the strips to at least the level of the wavy lines, but do not allow the urine level to pass above the arrows.
  6. Replace the cap, place the card on a flat, nonabsorbent surface and start the timer.
  7. Read the drug-screen results at five minutes.

Important: Review the complete package insert before performing the test. A clean, dry urine collection container and timer are required but are not supplied with the test cards.

Understanding the Results

Negative Two colored lines appear for the applicable panel: one in the control region and one in the test region. Any visible test line, even a faint line, should be interpreted as negative.
Presumptive positive A control line appears, but no test line appears for the applicable drug panel. The analyte may be present at or above the stated cutoff.
Invalid No control line appears. Review the procedure and repeat the test using a new test card.

Preliminary screening only: This test provides a qualitative, preliminary analytical result. Presumptive positive results should be confirmed using a more specific analytical method. Gas chromatography/mass spectrometry is identified in the package insert as the preferred confirmatory method. Clinical consideration and professional judgment should be applied to all drug-screening results.

Instructions and Product Documents

Frequently Asked Questions

Which drugs does DS130AC425 screen for?

It screens human urine for amphetamine, barbiturates, benzodiazepines, cocaine metabolite, MDMA, methamphetamine, methadone, opiates, phencyclidine and marijuana metabolite.

Is DS130AC425 CLIA-waived?

No. The exact DS130AC425 dip-card configuration is classified as CLIA moderately complex and should not be represented as CLIA-waived.

Is this an over-the-counter drug test?

This product should not be marketed as an OTC test. The package insert identifies the test for healthcare professionals, including professionals at point-of-care sites.

How quickly should the results be read?

The drug-screen results should be read at five minutes, following the instructions supplied with the product.

Does this configuration include specimen-validity testing?

No. The DS130AC425 configuration does not include adulteration or specimen-validity test pads.

Does the box include a urine collection cup?

No. A clean, dry specimen collection container is required but is not provided with the test cards.

Does a faint test line mean the result is negative?

Yes. Any visible colored line in the test region should be interpreted as negative, even when the line is faint. A control line must also appear for the result to be valid.

Does a presumptive positive result require confirmation?

Yes. This product provides preliminary qualitative screening results. A more specific analytical method should be used to obtain a confirmed result.

How should the test cards be stored?

Store the test cards in their sealed pouches at 36–86°F (2–30°C). Do not freeze them, and do not use a test after the expiration date printed on its sealed pouch.

Additional information

Weight 2 lbs
Dimensions 6 × 5 × 3 in

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