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CE OPI Opium Urine Rapid Test Kit Strip Cassette for Drug of Abuse Urine Test

Basic Information
Place of Origin: Foshan, China
Brand Name: Dewei
Certification: CE, ISO
Model Number: OPI-DU02
Minimum Order Quantity: 1000
Price: UD$0.1-US$0.4
Packaging Details: 40 tests/box, 1000 tests/carton
Delivery Time: 5-20 working days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 600000 tests/week
Detail Information
Shelf Life: 24 Month Specimen: Urine
Testing Time: 5-10 Minutes Test Drug Type: OPI
Test Format: Cassette OEM: Available
Export Port: Guangzhou, Shenzhen Principle: Immunoassay
High Light:

Urine rapid test strip cassette


OPI rapid test strip cassette


FDA rapid test cassette

Product Description

CE OPI Opium Urine Rapid Test Kit Strip Cassette for Drug of Abuse Urine Test




DOA Identifier Calibrator Cut-off Level
Opiate 2000(OPI) Morphine 2000ng/mL


This assay provides only a preliminary analytical test result. Gas Chromatography/Mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to Opiate 2000 (OPI) of abuse test result, particularly when preliminary positive results are indicated.


Opiate (OPI) Rapid Test is a rapid yields a positive result when the concentration of Opiates in urine exceeds 2000ng/mL.


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 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.



Preliminary positive (+) Only one colored band appears, in the control region (C), n
o 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.


Manufacturer by

Dewei Medical Equipment Co Ltd


Contact Details
Renee Zou

Phone Number : +8618028779938

WhatsApp : +8615267039708