Accutest 8 Panel Drug Test SplitCup+6 Adulteration Screens – 25/Box (AMP / BAR / BZO / COC / MET / OPI / PCP / THC) & (pH / SG / OX / Ni / Glut / CR)
$253.25 — or subscribe to save 5%
FDA 510(k) Cleared Drug Screen
8 Drug Panels + 6 SVT
25 Cups per Box
25 test cups per box • $10.13 per cup
The ACCUTEST® SplitCup is a self-contained professional urine drug-screening cup with a separate split-specimen chamber and key-activated testing. Reference DS208 screens for eight drugs or drug classes and includes six specimen-validity tests that help assess urine-sample integrity.
- Drug panels: AMP, BAR, BZO, COC, MET, OPI, PCP and THC
- Specimen-validity screens: pH, SG, OX/PCC, NIT, GLUT and CR
- Read specimen-validity screens between 3 and 5 minutes
- Read drug-screen results at 5 minutes
- Includes a temperature strip, security seal and separate specimen chamber
| 1-5 | 6-10 | 11+ |
| $253.25 | $232.99 | $220.33 |
ACCUTEST 8-Panel SplitCup Overview
The ACCUTEST® 8-Panel SplitCup is a professional-use lateral-flow immunoassay for the simultaneous qualitative screening of multiple drugs and drug metabolites in human urine. The self-contained split-cup design keeps a separate portion of the specimen available and allows the drug test to be activated with the supplied key when the operator is ready.
Reference DS208 screens for amphetamine, barbiturates, benzodiazepines, cocaine, methamphetamine, opiates, phencyclidine and marijuana. It also includes six semi-quantitative specimen-validity tests for pH, specific gravity, oxidants/PCC, nitrite, glutaraldehyde and creatinine to help assess specimen integrity.
FDA 510(k) Cleared Drug Screen
8 Drug Panels
6 Specimen-Validity Tests
Features and Benefits
Self-contained urine collection and drug-screening cup
Separate testing chamber helps preserve a split specimen
Key activation allows the operator to begin testing when ready
Drug-screen results are read at 5 minutes and remain stable for up to 60 minutes
Six specimen-validity indicators are read between 3 and 5 minutes
Built-in procedural control helps verify adequate specimen migration
Fahrenheit temperature strip helps support specimen-validity procedures
No instrument or additional reagent is required for the rapid screen
Product Details
DS208
DTK-109086
25 Cups per Box
Human Urine
Drug Panels and Cutoffs
| Drug or Drug Class | Abbreviation | Cutoff |
|---|---|---|
| Amphetamine | AMP | 1,000 ng/mL |
| Barbiturates | BAR | 300 ng/mL |
| Benzodiazepines | BZO | 300 ng/mL |
| Cocaine metabolite | COC | 300 ng/mL |
| Methamphetamine | MET | 1,000 ng/mL |
| Opiates | OPI | 2,000 ng/mL |
| Phencyclidine | PCP | 25 ng/mL |
| Marijuana metabolite | THC | 50 ng/mL |
Drug detection windows vary substantially with the substance, dose, frequency and duration of use, specimen concentration, individual metabolism and other biological factors. A detection window cannot determine impairment or the exact time a substance was used.
Specimen-Validity Screens
| Screen | Abbreviation | Purpose |
|---|---|---|
| pH | pH | Checks for unusually acidic or alkaline urine |
| Specific gravity | SG | Helps assess specimen dilution |
| Oxidants/PCC | OX/PCC | Screens for oxidizing agents, including pyridinium chlorochromate |
| Nitrite | NIT | Screens for elevated nitrite associated with certain commercial adulterants |
| Glutaraldehyde | GLUT | Screens for an aldehyde not normally present in urine |
| Creatinine | CR | Helps assess dilution and whether the specimen is consistent with human urine |
The specimen-validity pads provide semi-quantitative screening information that may help assess sample integrity. They do not by themselves prove intentional adulteration. The package insert states that specimen-validity testing does not require FDA review; the FDA-clearance statement applies to the drug-screening component.
How to Use the SplitCup
Prepare: Allow the sealed test cup, specimen and controls to reach 59–86°F (15–30°C). Open the pouch and use the cup promptly.
Collect: Twist the key from the center of the cap, collect the urine specimen and close the lid firmly until it clicks.
Seal: Date and initial the security seal, then place it across the cup lid according to the package insert.
Activate: Place the cup on a flat surface, push the key fully into the closed position and start the timer.
Read specimen validity: Compare the validity pads with the supplied color chart between 3 and 5 minutes.
Read the drug screen: Remove the result-covering label and interpret the drug strips at 5 minutes. Follow the package insert for complete instructions.
Understanding Drug-Screen Results
Negative: A control line and a test line appear for the applicable drug panel. Any visible test line, even a faint one, is interpreted as negative.
Preliminary positive: A control line appears but no test line appears for the applicable drug panel. Confirm preliminary positive results with a more specific laboratory method.
Invalid: No control line appears. Review the procedure and repeat testing with a new cup.
This test provides a preliminary qualitative screening result only. A more specific alternate method, such as GC/MS, must be used to obtain a confirmed analytical result. Clinical consideration and professional judgment should be applied to every result.
Storage and Handling
Store sealed test cups at 36–86°F (2–30°C)
Keep each test in its sealed pouch until use
Do not freeze and do not use beyond the expiration date printed on the pouch
When using specimen-validity testing, test the urine promptly and follow the insert’s specimen-storage limits
Instructions and Product Documents
Frequently Asked Questions
Which drugs does the DS208 SplitCup screen for?
It screens for amphetamine, barbiturates, benzodiazepines, cocaine metabolite, methamphetamine, opiates, phencyclidine and marijuana metabolite at the cutoffs shown in the product table.
Which specimen-validity indicators are included?
The DS208 configuration includes pH, specific gravity, oxidants/PCC, nitrite, glutaraldehyde and creatinine. These semi-quantitative screens may help identify an abnormal or potentially compromised urine specimen.
How quickly are results available?
Read the specimen-validity pads between 3 and 5 minutes and read the drug-screen strips at 5 minutes. The package insert states that drug-screen results remain stable for up to 60 minutes.
Is the DS208 intended for home use?
No. The supplied package insert identifies the test for healthcare professionals, including professionals at point-of-care sites. This page does not identify DS208 as an over-the-counter self-test.
Does an abnormal specimen-validity result prove adulteration?
No. The validity pads provide screening information that can help assess urine-sample integrity. Follow your organization’s drug-free workplace policy and the package insert when a specimen produces an abnormal validity result.
Does a preliminary positive drug result require confirmation?
Yes. The test provides a preliminary analytical result. The package insert states that a more specific alternate chemical method, such as GC/MS, must be used to obtain a confirmed analytical result.
What does a faint test line mean?
A visible test line is interpreted as negative even when it is faint, provided the control line appears and the test was performed and read according to the package insert.
How many test cups are included?
This DS208 configuration is sold as 25 test cups per box.
Compare Urine Drug Test Cups
Browse additional urine drug-test cup configurations by panel count, screened analytes and available specimen-validity indicators.
Looking for Workplace Drug-Testing Information?
Review federal workplace drug-testing resources and confirm the requirements that apply to your organization, industry and jurisdiction.
Additional information
| Weight | 5 lbs |
|---|---|
| Dimensions | 16 × 14 × 5 in |
