Adresse: 90-94 Tianfeng Road, Jimei North Industrial Park, Xiamen, Fujian, P.R.China
Telefon: +86-592-3965107
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Package
BOSON Rapid Drug Test are properly packed with pouch, giftbox, and carton.
Cassette: 25 Tests/Box; 40 Tests/Box;
Strip: 50 Tests/Box; 100 Tests/Box;
Rapid OPI II Test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of opiate metabolites in human urine specimens.
PROCEDURE
For OPI II Test Strip (Catalog Number:1L12S3)
1. Bring test device and specimens to the room temperature (15-28C) if they have been refrigerated..
2. Remove the test strip from the sealed foil pouch and use it as soon as possible.
3. With arrows pointing toward the urine specimen, immerse the sample pad end of the test strip in the urine specimen..
4. Hold the test strip in a vertical position for at least 10 seconds.
5. Remove the test strip from the urine. While removing the test strip, run the edge of the strip against the rim of the specimen container to remove excess urine.
6. Place the test strip on a clean, dry and non-absorbent surface.
7. Read the results at 5 minutes after adding the sample.
For OPI II Test Card (Catalog Number:1L12C3)
1. Bring all materials and specimens to room temperature.
2. Remove the test card from the sealed foil pouch.
3. Label the test card with specimen identity on the ID ____ area of the cassette.
4. Place the test card on a flat horizontal surface.
5. Using the transfer pipet to draw up the sample.
6. Hold the pipette in a vertical position over the sample well marked as S on the test card and drip 2-3 drops (80-120ml) sample into the sample well.
7. Read the results at 5 minutes after adding the sample.
Note: Do not interpret the results after 10 minutes.
INTERPRETATION OF RESULTS
Negative:
Two colored bands form. The appearance of two colored bands, one in test line zone and the other in control line zone, indicates negative result for that particular test(s). The negative result does not indicate the absence of drug and their metabolites in the specimen, it only indicates the level of tested drug and their metabolites in the specimen is less than cut-off level.
Positive:
One colored band forms. One colored band appears in control line zone. No colored band is found in test line zone. This is an indication the level of tested drug and their metabolites in the specimen is above the cut-off level.
Invalid:
If there is no colored band in control line zone of any strip, the test result is invalid. Retest the sample with a new device.
Note: A borderline() in test line zone should be considered negative result.
Sensitivity
The cut-off concentration (sensitivity level) of Rapid OPI II Test is determined to be: OPI II 2000ng/ml.
Rapid TnI Test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of cardiac troponin I (cTnI) in human serum, whole blood or plasma specimens as an
Package
BOSON Rapid Drug Test are properly packed with pouch, giftbox, and carton.
Cassette: 25 Tests/Box; 40 Tests/Box;
Strip: 50 Tests/Box; 100 Tests/Box;
Rapid THC Test
Package
10cups/box, 100cups/carton.
Rapid Drugs Of Abuse/Alcohol Test Cup, hereinafter refered to as DOA/Alcohol Test Cup, is an immunochromatography based one step in vitro t
Package
10cups/box, 100cups/carton.
Rapid Drugs Of Abuse/Alcohol Test Cup, hereinafter refered to as DOA/Alcohol Test Cup, is an immunochromatography based one step in vitro t
Rapid AFP Test is an immunochromatography based one step in vitro test. It is designed for the rapid qualitative determination of AFP in serum , plasma or whole blood specimens to aid in the dia
Certificate: ISO13485, FSC
INTENDED USE
Rapid Adeno/Rota Virus Antigen Combo Test is an in vitro qualitative immunochromatographic assay for the rapid detection of adenovirus rotavirus antigens
Rapid Adenoirus Antigen Test
Certificate: ISO13485, FSC
INTENDED USE
Rapid Adenovirus Test is an in vitro qualitative immunochromato-graphic assay for the rapid detection of adenovirus an
Rapid Cardiac Panel test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of cardiac troponin I (cTnI), CK-MB and Myoglobin in human serum, plasma
Rapid CEA Test Card is an immunochromatographic assay for the qualitative determination of Carcinoembryonic Antigen (CEA) in human serum, plasma or whole blood specimens.
This device is intended as a
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