5 Panel Drug Test Cup CLIA Waived with Adulterants 25/Box
Brand : Healgen Scientific
Multi-Panel CLIA Waived Drug Screening Test Cup 5-Panel with 3 Built-In Adulteration Tests
This High Quality CLIA Waived drug test cup is an easy, fast, qualitative, competitive binding immunoassay method for screening without the need of instrumentation. 
The Multi-Panel Drug Test Cup is a No Step, fully integrated self contained multi-drug screening cup. No tipping or turning required. Read results
in 5 minutes. The cup is FDA Cleared and CLIA Waived. This non-branded cup is a fast visual, competitive panel immunoassay that can be used for the
simultaneous, qualitative detection of multiple drug metabolites at specific cutoff levels in human urine.
Features & Benefits
- CLIA Waived
- FDA 510(K) Approved
- Health Canada Approved
- CE Marking - Meets all European Conformity Standards
- Includes Built-In Adulteration tests for Specific Gravity (SG), Oxidants (OX) and pH Level (pH)
- Sold in boxes of 25 tests
- New "Click Seal" cap!
- No step cup
- Up to 99% Accurate
- Dual scale Temperature Strip verifies if urine is "fresh" and not diluted
- Adheres to the SAMHSA Cutoff Levels
- Immediate Results
- Shelf-life up to 24 months
- New easy to open top for the confirmation lab
Download & Print Reference Materials
Multi-Panel CLIA Waived Drug Test Package Insert
Multi-Panel CLIA Waived Drug Test Instruction Sheet
Six Panel Configuration(s)
| Item Number | Drugs Tested | Adulterants Tested |
| HCDOA-154A3 | AMP, COC, OPI, PCP, THC | OX, SG, pH |
| HCDOA-254A3 | AMP, COC, MET, OPI, THC | OX, SG, pH |
| HCDOA-654A3 | BZO, COC, mAMP, OPI, THC | OX, SG, pH |
SAMSHA Approved CLIA Waived Drug Panel Options
| Drug Name | Abbreviation | Cutoff Level | Minimum Detection Time in Urine* | Maximum Detection Time in Urine* | Calibrator |
| Amphetamine | AMP | 1000 ng/ml | 2-7 hours | 2-4 days | D-Amphetamine |
| Barbiturates | BAR | 300 ng/ml | 2-4 hours | 1-3 weeks | Secobarbital |
| Benzodiazepines | BZO / BZD | 300 ng/ml | 2-7 hours | 1-4 days | Benzoylecgonine |
| Buprenorphine | BUP | 10 ng/ml | 2-3 hours | 1 day | Buprenorphine |
| Cocaine | COC | 300 ng/ml | 1-4 hours | 2-4 days | Benzoylecgonine |
| Ecstasy | MDMA | 500 ng/ml | 1-3 days | 1-2 days | D,L- Methylenedioxy-methamphetamine |
| Marijuana | THC | 50 ng/ml | 2 hours | up to 40 days | 11-nor-Δ9-THC-9 COOH |
| Methadone | MTD / MAD | 300 ng/ml | 3-8 hours | 1-3 days | Methadone |
| Methamphetamine | mAMP / MET | 1000 ng/ml | 2-7 hours | 2-4 days | D-Methamphetamine |
| Morphine | MOP / OPI-300 | 300 ng/ml | 2 hours | 2-3 days | Morphine |
| Opiates | OPI | 2000 ng/ml | 2 hours | 2-3 days | Morphine |
| Oxycodone | OXY | 100 ng/ml | 1-3 hours | 1-2 days | Oxycodone |
| Phencyclidine | PCP | 25 ng/ml | 4-6 hours | 7-14 days | Phencyclidine |
| Propoxyphene | PPX | 300 ng/ml | 1-2 days | N/A | Propoxyphene |
| Tricyclic Antidepressants | TCA | 1000 ng/ml | 8-12 hours | 2-7 days | Nortriptyline |
| * Detection times are not guaranteed. Reference configuration above for included drug panels. | |||||
Optional CLIA Waived Drug Panels (call 404-840-8900 for more information)
| Drug Name | Abbreviation | Cutoff Level | Minimum Detection Time in Urine* | Maximum Detection Time in Urine* | Calibrator |
| Amphetamine | AMP | 500 ng/ml | 2-7 hours | 2-4 days | D-Amphetamine |
| Cocaine | COC | 150 ng/ml | 1-4 hours | 2-4 days | Benzoylecgonine |
| EDDP | EDDP | 300 ng/ml | 1-4 hours | 2-4 days | 2-Ethylidene-1,5-dimethyl-3,3-dipheylpyrrolidine |
| Methamphetamine | mAMP / MET | 500 ng/ml | 2-7 hours | 2-4 days | D-Methamphetamine |
| * Detection times are not guaranteed. Reference configuration above for included drug panels. | |||||
Adulterant Tests (Specimen Validity Tests) Summary 
pH Level (pH) Tests for the presence of acidic or alkaline adulterants in urine. Normal pH levels should be in
the range of 4.0 to 9.0. Values below pH 4.0 or above pH 9.0 may indicate the sample has been altered. Urine pH below 4 or above 9 indicates adulteration
with an acidic or basic compound.
Specific Gravity (S.G.) Tests for sample dilution. Normal levels for specific gravity will range from 1.003 to 1.030.
Specific gravity levels of less than 1.003 or higher than 1.030 may be an indication of adulteration or specimen dilution. In the presence of an indicator,
the colors changes from dark blue to blue-green in urine of low ionic concentration to green and yellow-green in urine of higher ionic concentration.
Oxidants (OXI) Tests for the presence of oxidizing agents such as bleach and peroxide in the urine.
Nitrites (NIT) Tests for commercial adulterants such as Klear and Whizzies. Normal urine specimens should contain
no trace of nitrite. Positive results for nitrite usually indicate the presence of an adulterant.
Creatinine（CRE) Creatinine is one way to check for dilution and flushing, which are the most
common mechanisms used in an attempt to circumvent drug testing. Low creatinine may indicate dilute urine.
Glutaraldehyde（GLUT) Tests for the presence of an aldehyde. Glutaraldehyde is not normally
found in a urine specimen. Detection of glutaraldehyde in a specimen is generally an indicator of adulteration.
TransMed Company offers the following optional Forensic Use Only (FUO) Panels: K2/Spice, EtG, Tramadol and Fenytanyl
This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed
analytical result. Gas Chromatography/Mass Spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment
should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated.
