FDA CE Multi DOA Rapid Diagnostic Test Kits Dipcard Panel Urine Sample Test

Basic Information
Place of Origin: Foshan, China
Brand Name: Dewei
Certification: CE FDA ISO
Model Number: MDD-D52
Minimum Order Quantity: 1000
Price: $0.3-$2.5
Packaging Details: 1 test per pouch, 25 or 50 tests per box, 1000 tests per carton.
Delivery Time: 10-20 working days
Payment Terms: T/T, Western Union, MoneyGram
Detail Information
Material: Paper, Colloidal Gold Specimen: Urine
Test Target: 2-12 DOA Shelf Life: 2 Years
Test Time: 5-10 Mins Test Format: Dipcard
High Light:

FDA Urine Sample Rapid Test Kit


Dipcard Panel rapid diagnostic test kits


Multi DOA rapid diagnostic test kits

Product Description

FDA CE Multi-DOA Rapid Test Kit Dipcard Panel COC AMP THC BENZO OPI Urine Sample Test


2-15 combination of the following drugs:AMP/ BAR/ BUP/ BZO/ COC/ COT/ ETG/ FYL/ K2/ KET/ MAM/ MDMA/MET/ MOP300/ MQL Rapid Multi-Drug 2-15 Test is a rapid, screening test for the qualitative detection of multiple drugs and drug metabolites in human urine at specified cut off levels. For professional use only. For in vitro diagnostic use only.


DOA (Identifier) Calibrator Cut-off lever
Cocaine (COC)
Benzoylecgonine 300 ng/mL
Amphetamine (AMP)
d-Amphetamine 1000ng/mL
marijuana (THC)
50 ng/mL
Benzodiazepines (BZO
300 ng/mL
Opiate 2000 (OPI)


Test must be in room temperature (15ºC to 30ºC)
1. Donor collects urine specimen in a urine cup.
2. Open the sealed pouch by tearing along the notch. Remove the test cassette from the pouch and place it on a level surface.
3. Hold the sample dropper vertically, and add exactly three drops of the urine specimen into the sample well.
4. The result should be read at 5 minutes. Do not interpret the result after 10 minutes. See the illustration below.

FDA CE Multi DOA Rapid Diagnostic Test Kits Dipcard Panel Urine Sample Test 0


Preliminary positive (+) Only one colored band appears, in the control region (C). No colored band appears in the test region (T).
Negative (-) Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
Invalid Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded.
Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.


Drug Test
Leaflet with instruction for use


The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch
The test must remain in the sealed pouch until use
Keep away from direct sunlight, moisture and heat
Do not freeze.
Care should be taken to protect the components of the kit from contamination.
Do not use if there is evidence of microbial contamination or precipitation.
Biological contamination of dispensing equipment, containers or reagents can lead to false results.


【Manufactured by】
5th floor, No. 4 building, Shiyou Industrial Park, Jun'an , Shunde, Foshan, China 528329

Contact Details
Renee Zou

Phone Number : +8618028779938

WhatsApp : +008615267039708