Multi-Drug Test Cup
Multi-drug 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.
The tests are intended for In Vitro Diagnostics use. They are intended for prescription use including point of care sites and over-the-counter use.
|Product Name||Multi-Drug Test Cup|
|Brand Name||CIBIO® or OEM|
|Format||Multi-drug Test Cup|
|Kit Contents||1. Test Cup|
|3. Instruction for use|
|Assay Type||Qualitative Detection|
|Panels Content||2-18 panel drug test for Cup|
|6 adulterant strips optional for cup format|
|Certificates||ISO 13485, FDA 510K , Clia-Waived|
|Storage Temperature||4-30 degree centigrade|
|Shelf Life||2 years ( 24 months )|
|Delivery time||15-30 days|
|OEM Services||Pouch, Box, Label, Insert|
|Loading Port||Guangzhou or Shenzhen, China|
|Drug Tests Available and Cut-off Levels|
|1||Amphetamine (AMP)||500/ 1000 ng/mL|
|2||Barbiturates (BAR)||300 ng/mL|
|3||Benzodiazepines (BZO)||300 ng/mL|
|4||Buprenorphine (BUP)||10 ng/mL|
|5||Cocaine (COC)||150/ 300 ng/mL|
|6||Marijuana (THC)||25/ 50 ng/mL|
|7||Methamphetamine (MET)||500/ 1000 ng/mL|
|10||Morphine 300 (MOP)||300ng/mL|
|11||Opiate 2000 (OPI)||2000ng/mL|
|15||Tri-cyclic Antidepressants (TCA)||1000ng/mL|
|16||Ethyl -glucuronide(ETG)||300 or 500ng/mL|
|18||Synthetic Marijuana (K2)||50ng/mL|
|Optional Adulterant Strips: CR/OX/pH/S.G/NIT/GLU|
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.
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
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.