Audited Supplier
Methadone Metabolite (EDDP) Rapid Test is an immuno-chromatographic assay for the qualitative determination of the presence of Methadone Metabolite(EDDP) listed in the table below.
| Drug(Identifier) | Calibrator | Cut-off level |
Methadone Metabolite (EDDP) | 2- ethylidene-1, 5-dimethyl-3, 3- diphenylpyrrolidine(EDDP) | 300 ng/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 Methadone Metabolite(EDDP) of abuse test result, particularly when preliminary positive results are indicated.
EDDP(2-Ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine) is the primary metabolite of methadone. Methadone is a synthetic analgesic drug that is originally used in the treatment of narcotic addicts. The detection of EDDP is more beneficial than traditional methadone screening since EDDP exists only in urine from individuals that ingested methadone. The tampering of specimens by spiking the urine with methadone can be prevented. Secondly, renal clearance of EDDP is not affected by urinary pH, therefore the EDDP test provides a more accurate result of methadone ingestion than the methadone parent screen.
- Drug Test.
- Desiccant
- 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.
- Test must be in room temperature (15ºC to 30ºC)
- Donor collects urine specimen in a urine cup.
- Open the sealed pouch by tearing along the notch. Remove the test from the pouch and place it on a level surface.
- Hold the sample dropper vertically, and add exactly three drops of the urine specimen into the sample well.
- 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). 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.
About Us
Dewei Medical Equipment Co., Ltd. is a high-tech enterprise specialized in developing and marketing of Medical Consmuables like Clinical Laboratory analyzer and reagents, Hematology Analyzer and Reagents, Washing Solutions, Urine Sediment Reagents and DNA/RNA Preservation Kits.
During the special period, Dewei also develop the reagent kits, like Virus Transport Medium with swab, Rapid test and Saliva Collection Kits.
Dewei products are widely used in hospital clinics, disease control centers, blood banks, veterinary clinics, scientific research center and college laboratories.
15% annual sales amount is devoted R&D department.
With professional R&D team, Dewei is continuously making new achievements on innovation, gaining numbers of national invention patents and professional technical awards. Meanwhile, Dewei focuses on the improvement of technology to guarantee product quality and pursue product performance.
Certificate
Production Workshop
Exhibition
Our Team
Transportation
