One Step Muti-Drug-M D 01

• Product Name:

  One Step Muti-Drug-M D 01

• Category: Medical devices/Diagnostic Devices
• Package: carton
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• Product Detials:One Step Multi-Drug Screen Test Panel(Urine) Instruction Sheet for testing of any combination of the following drugs: AMP, BAR, BZO, COC, MET, MOP, MID, PCP, TCA, THC A rapid, one step screen test for the simultameous, qualitative detection of multiple drugs and metabolites in human urine For professional in vitro diagnostic use only. INTENDED USE The Multi-Drugs One Step Screen Test Panel(Urine) is a lateral flow chromatographic immunoassay for the qualitative detection of Amphetamine, Barbiturates, Benzodiazepines, cocaine, Methamphetamine, Morphine, Mathadone, Phencyclidine, Tricyclic Antidepressants and Marijuana in human urine. SUMMARY Urine based screen tests for multiple drugs of abuse range from simple immunoassay tests to complex analytical procedures. The speed and sensitivity of immunoassays have made them the most widely accepted method to screen urine for multiple drugs of abuse. The Multi-drugs One step Screen Test Panel (Urine) is a rapid urine visual, competitive screen immunoassay that can be used for the simultaneous, qualitative detection of Amphetamine, Barbiturates, Benzodiazepines, Cocaine, Methamphetamine, Morphine, Mathadone, Phencyclidine, Tricyclic Antidepressants and Marijuana in human urine at the following cut-off concentrations: 1000 gn/mL Amphetamine, 300ng/mL, Secobarbital(Barbiturates metabolite), 300 ng. ML Oxazepam (Benzodiazepines metabolite), 300ng/mL Benzoylecgonine (Cocaine metabolite), 1000ng/mL Methamphetamine, 300 ng/mL Morphine, 300 ng. ML Methadone, 25 ng/mL Phencyclidine, 1000 ng. ML Tricyclic Antidepressants, 50ng/mL 11-nor=9-THC-9 COOH(THC) without the need of instrument. PRECAUTIONS For in vitro diagnostic use only. Do not use after the expiration date. The test panel should remain in the sealed pouch until use. All specimens should be considered potentially hazardous and handled in the same manner as an infectious agent. Then used test device should be discarded according to federal, state and local regulations. Humidity and temperature can adversely affect results. STORAGE AND STABILITY Store as packaged in the sealed pouch at 2-30 Centigrade, The test panel is stable through the expiration date printed on the scaled pouch. The test panel must remain in the scaled pouch until use. DO NOT FREEZE. Do not use beyond the expiration date. SPECIMEN COLLECTION AND PREPARATION Urine Assay The urine specimen must be collected in a clean and dry container. Urine collected at any time of the day may be used. Urine specimens exhibiting visible precipitates should be centrifuged, filtered, or allowed settle to obtain a clear supernatant for testing. Specimen Storage Urine specimens may be stored at 2-8 Centigrade for up to 48 hours prior to assay. For prolonged storage, specimens may be frozen and stored below -2 Centigrade. Frozen specimens should be thawed and mixed before testing. MATERIALS Materials Provided Test panels Package insert Materials Required But Not Provided Specimen collection container Timer INTERPRETATION OF RESULTS (Please refer to the illustration above) NEGATIVE: Two lines adjacent to each drug name appear. One red line should be in the control region of the specific drug test, and another apparent red or pink line adjacent to each drug test should be in the test region(T) of the specific drug test. More Product Features HS Code: 38220010 Model NO.: M D 01 Standard: CE Productivity: 50,000,000 Pcs/Year Origin: China Packing: carton Min. Order: 10000pcs Transportation: by air Company: Medcare Biotech Co., Ltd.