Description

Multi Drug Abuse Test Cup

Multi-drug abuse Test Cup is a rapid, screening test for the qualitative detection of multiple drugs and drug metabolites in human urine at specified cut off levels. This Cup simultaneously detects up to 18 different substances.

For professional use. For in vitro diagnostic use only.

Product Name	Drug Addiction Test Cup 1-18 panels
Brand Name	CIBIO® or OEM
Format	Multi-drug Test Cup
Methodology	Colloidal Gold
Kit Contents	1. Test Cup
	2. Desiccant
	3. Instruction for use
Assay Type	Qualitative Detection
Specimen	Urine
Panels Content	2-18 panel drug test for Cup
	6 adulterant strips optional for cup format
Certificates	ISO 13485, FDA 510K , Clia Waived, CE
Accuracy	Over 99%
Storage Temperature	4-30 degree centigrade
Shelf Life	2 years ( 24 months )
Delivery time	15-30 days
OEM Services	Pouch, Box, Private Label, Insert
Loading Port	Guangzhou or Shenzhen, China

Toxicology Urine test list

	Product Description	Abbreviations	Cut-off Level	Qualification
1	Amphetamine	AMP	1000 ng/mL	CE	FDA 510K, CLIA-waived
2	Barbiturates	BAR	300 ng/mL	CE	FDA 510K, CLIA-waived
3	Buprenorphine	BUP	10 ng/mL	CE	FDA 510K, CLIA-waived
4	Benzodiazepines	BZO	300 ng/mL	CE	FDA 510K, CLIA-waived
5	Cocaine	COC	300 ng/mL	CE	FDA 510K, CLIA-waived
6	Cotinine	COT	200 ng/mL	CE
7	Ethylglucuronide	ETG	500 ng/mL	CE
8	Fentanyl	FYL	200 ng/mL	CE
9	Fentanyl	FYL	1 ng/mL		FDA 510K
10	Synthetic Cannabinoid	K2	50 ng/mL	CE
11	Ketamine	KET	1000 ng/mL	CE
12	6-Acetylmorphine	6-MAM	10 ng/mL	CE
13	Methylenedioxymethamphetamine – ecstasy	MDMA	500 ng/mL	CE	FDA 510K, CLIA-waived
14	Methamphetamine	MET	1000 ng/mL	CE	FDA 510K, CLIA-waived
15	Morphine	MOP	300 / 2000 ng/mL	CE	FDA 510K, CLIA-waived
16	Methadone	MTD	300 ng/mL	CE	FDA 510K, CLIA-waived
17	Opiate 2000	OPI	2000 ng/mL	CE
18	Oxycodone	OXY	100 ng/mL	CE	FDA 510K, CLIA-waived
19	Phencyclidine	PCP	25 ng/mL	CE	FDA 510K, CLIA-waived
20	Propoxyphene	PPX	300 ng/mL	CE	FDA 510K, CLIA-waived
21	Tri-cyclic Antidepressants	TCA	1000 ng/mL	CE	FDA 510K, CLIA-waived
22	Marijuana	THC	50 ng/mL	CE	FDA 510K, CLIA-waived
23	Marijuana	THC	20 / 50ng/mL		FDA 510K, CLIA-waived
24	Tramadol	TRA	200 ng/mL	CE
25	Xylazine	XYL	1000 ng/mL
26	Methaqualone	MQL	300 ng/mL	CE
27	Carisoprodol	SOMA	1000 ng/mL
28	Methcathinone	MCAT	500 ng/mL
29	Lysergic Acid Diethylamide	LSD	20 ng/mL
30	Kratom	KRA	500 ng/mL
31	3,4-Methylenedioxypyrovalerone	MDPV	1000 ng/mL

Optional Adulterant Strips: CR – Creatinine, OX – Oxidants, pH – Acidic or Alkaline, S.G – Specific Gravity, NIT – Nitrite, GLU – Glutaraldehyde

Advantage

• Easy to use and easy to read the result
• High accuracy over 99% and high speed
• Lid tighten indicator design
• Minimum fill volume only 20ml
• Results stable up to 30 minutes
• 28 drug configurations avaliable
• 24 months shelf life
• ISO 13485, CE Rep, Clia waived, FDA 510k
• Detect Eighteen drugs simultaneously
• Each cup has a individually sealed pouch
• Temperature strip that detect temperature of fresh sample for Specimen Validity Testing
• CLIA Waived for home use
  

Ideal for / Applications

Home drug testing
Workplace testing
School drug testing
Lab screen testing
Pre-employment testing
Pain management
Law enforcement drug testing
Criminal justice drug testing

How to do the test ?

Test must be in room temperature 59-86°F (15-30°C).

1. After the urine has been collected, tighten lid to the indicator, and place the test cup on a flat surface.
2. Read temperature immediately to verify that urine temperature is within the acceptable range. 90–100°F (32–38 °C)
3. Peel off label and read the results. The drug test results should be read at 5 minutes. The drug test results remain stable for up to thirty minutes.

Reading The Results

Preliminary positive (+)
A rose-pink band is visible in each control region. If no color band appears in the appropriate test “T” region, a preliminary positive result is indicated for the corresponding drug of that specific test zone.

Negative (-)
If a rose-pink band is visible in each control region and the appropriate test “T” region, it indicates that the concentration of the corresponding
drug of that specific test zone is absent or below the detection limit of the test.

Invalid
If a color band is not visible in the control “C” region or a color band is only visible in the test “T” region, the test is invalid. Another test should opened and run to re-evaluate the specimen. If test still provides an invalid result, please contact the distributor from whom you purchased the product. When calling, be sure to provide the lot number for the test.

Q&A

Qus: How do rapid drug tests work?

Rapid drug tests detect the presence of drugs and drug metabolites in human urine at specified cut off levels in minutes. When a detection strip is wetted with  urine specimen, the specimen reacts with the reagents and antigens on the strip and produces a color reading so you can interpret a positive or negative result.

Qus: What is the difference between a Dip Card Test and an Integrated Cup Test?

The Dip Card is dipped into a urine specimen to get results. A cup is a convenient way that the specimen is collected in the cup and tested there as well. There is no handling of the specimen.

Qus: What is the shelf life of your drug testing products?

The rapid drug test products have a shelf life of 24 months from manufacturing date. The expiration date is on every individual pack.

Qus: The drug line is lighter than the control line. Does this mean some drug is present?

No. Any line next to the word Drug or the drug abbreviation (depending on the test you have purchased), no matter how dark or light, is considered a Negative Result and no further testing is required.

Qus: Why is Urine Testing the Most Frequently Used Method for Drug Testing?

Businesses choose to drug test their workers and new job applicants to reduce the risk of workplace drug use and relevant hazards. While all drug test types, like hair follicle, blood, and saliva, have their benefits, urine drug testing is the most flexible and customizable.