Quantity	Price per Box (25)	Each Price
Buy 1 - 3	$74.25	$2.97
Buy 4 - 7	$72.00	$2.88
Buy 8 - 11	$69.75	$2.79
Buy 12 - 19	$68.00	$2.72
Buy 20 or above	$65.50	$2.62

Quantity

Price per Box (25)

Each Price

Buy 1 - 3

$74.25

$2.97

Buy 4 - 7

$72.00

$2.88

Buy 8 - 11

$69.75

$2.79

Buy 12 - 19

$68.00

$2.72

Buy 20 or above

$65.50

$2.62

Description
Other Details

6 Panel Drug Test Cup + 3 Adulterants, CLIA Waived

Multi-Panel CLIA Waived Drug Screening Test Cup 6-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
Includes "O-Ring seal" in cap for improved leak resistance
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
Item Number	Drugs Tested	Adulterants Tested
HCDOAV-264A3	AMP , BZO, COC, MET, 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. 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.

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. 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.

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

Per Each: