|Place of Origin:||Foshan, China|
|Certification:||US FDA, CE, ISO|
|Minimum Order Quantity:||1000|
|Packaging Details:||25 tests/box, 1000 tests/carton|
|Delivery Time:||5-20 working days|
|Payment Terms:||T/T, Western Union, MoneyGram|
|Supply Ability:||600000 tests/week|
|Shelf Life:||24 Month||Specimen:||Urine|
|Testing Time:||5-10 Minutes||DOA Type:||OPI|
|Export Port:||Guangzhou, Shenzhen||Principle:||Immunoassay|
Urine rapid test strip cassette,
OPI rapid test strip cassette,
FDA rapid test cassette
FDA CE DOA Opi Urine Rapid Test Cassette Kit Strip
|DOA Identifier||Calibrator||Cut-off Level|
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.
【INTERPRETATION OF RESULTS】
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.
Leaflet with instruction for use
【STORAGE AND STABILITY】
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.
Dewei Medical Equipment Co Ltd