Accu-Tell ®  Multi-Drug Saliva Rapid Test Cassette for AMP/MET/COC/OPI/THC/PCP/MTD/MDMA/OXY/COT/BZO/KET/6-MAM is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in saliva. This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) and gas chromatography/tandem mass spectrometry (GC/MS/MS) are the preferred confirmatory methods. Professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated. TEST PROCEDURE of Drug Metabolites Rapid Test Allow the test cassette, specimen, and/or controls to reach room temperature (15-30 °C) prior to testing. Instruct the donor to not place anything in the mouth including food, drink, gum or tobacco products for at least 10 minutes prior to collection. 1. Bring the pouch to room temperature before opening it. Remove the test from the sealed pouch and use it within one hour. Remove the collector from the sealed pouch and insert the sponge end of the collector into the mouth. Actively swab the inside of the mouth and tongue to collect oral fluid for a total of 3 minutes until the sponge becomes fully saturated. Gentle pressing the sponge between the tongue and teeth will assist saturation. No hard spots should be felt on the sponge when saturated. 2. Remove the collector from the mouth. Place saturated oral fluid collector into chamber and press sponge fully against the strainer to collect oral fluid.  Discard the collector.  Snap the cap shut on the collection chamber. 3. Place the test cassette on a clean and level surface.  Unscrew cap cover from the collection chamber.  Invert the collection chamber and transfer 3 drops of oral fluid (approximately 120 µL) into specimen well of the test cassette and start the timer.  Avoid trapping air bubbles in the specimen well. Place screw cap on the collection chamber. See illustration above.  We are Drug Of Abuse Rapid Tests Supplier.
Alcohol Urine Rapid Test Strip Accu-Tell® Alcohol Rapid Test Strip (Urine) is intended for use as a rapid method to detect the presence of alcohol in urine greater than 0.04%(40mg/dL). To confirm the concentration of positive specimens, an alternate, non-enzymatic technology such as headspace gas chromatography should be used. CATALOG Product Name Specimen Catalog No. Quantity per box Alcohol Strip Urine ABT-ACH-A188 100T/50T KEY POINTS Detection for:  Ehyl alcohol in human urine greater than 0.04%(40mg/dL); Reading time:  3 minutes; Relative Sensitivity:  96%; Relative Specificity:  100%; Agreement:  98%.  INTRODUCTION of Hot Sale Urine Rapid Test Strip Alcohol intoxication can lead to loss of alertness, coma, death and as well as birth defects. The BAC at which a person becomes impaired is variable. The United States Department of Transportation (DOT) has established a BAC of 0.02%(20mg/dL) as the cut-off level at which an individual is considered positive for the presence of alcohol. Determination of ethyl alcohol in urine, blood and saliva is commonly used for measuring legal impairment, alcohol poisoning, etc. Gas chromatography techniques and enzymatic methods are commercially available for the determination of ethyl alcohol in human fluids. ACCU-TELL ®  Alcohol Rapid Test Strip (Urine) is designed to detect ethyl alcohol in urine specimens.  INTENDED USE ACCU-TELL ®  Alcohol Rapid Test Strip (Urine) is intended for use as a rapid method to detect the presence of alcohol in urine greater than 0.04%(40mg/dL). The ACCU-TELL ®  Alcohol Rapid Test Strip (Urine) is intended for the detection of ethyl alcohol in human urine. To confirm the concentration of positive specimens, an alternate, non-enzymatic technology such as headspace gas chromatography should be used.  TEST PROCEDURE 1. Open the pouch package and remove the test strip. 2. Dipping the strip into the urine specimen for at least 20 seconds. 3. After wetting the reaction pad by urine specimen, immediately remove the strip from the urine specimen. 4. Read the alcohol test results at 3 minutes. Compare the color of the reaction pad with the color card to determine the relative urine alcohol level.
Product Name Specimen Catalog No. Quantity per box Alcohol Strip Saliva ABT-ACH-A187 100T/50T KEY POINTS Detection for:  Alcohol in human saliva at a cut-off concentration of 0.02% (20mg/dL); Reading time:  2 minutes; Agreement:  98%.  INTRODUCTION of Drug Of Abuse Rapid Tests Two-thirds of all adults drink alcohol.1However, alcohol intoxication can lead to loss of alertness, coma, death and birth defects. The blood alcohol concentration (BAC) at which a person becomes impaired is variable. The United States Department of Transportation (DOT) has established a BAC of 0.02%(20mg/dL) as the cut-off level at which an individual is considered positive for the presence of alcohol. Determination of ethyl alcohol in urine, blood and saliva is commonly used for measuring legal impairment, alcohol poisoning, etc. Gas chromatography techniques and enzymatic methods are commercially available for the determination of ethyl alcohol in human fluids. ACCU-TELL ®  Alcohol Rapid Test Strip (Saliva) is designed to detect ethyl alcohol in saliva specimens.  INTENDED USE ACCU-TELL ®  Alcohol Rapid Test Strip (Saliva) is a One Step method for the detection of Alcohol in human saliva at a cut-off concentration of 0.02% (20mg/dL). This assay provides only a qualitative, preliminary analytical test result. An alternate, non-enzymatic technology must be used in order to obtain a confirmed analytical result. Headspace gas chromatography is the preferred confirmatory method.  Allow the pouched strip to equilibrate to room temperature (15-27 °C) prior to testing. Abstain from placing anything in the mouth for fifteen (15) minutes prior to beginning the test. This includes non-alcoholic drinks, tobacco products, coffee, breath mints and food, etc 1.     Open the pouch package and remove the test strip. Observe the reactive pad on the end of the test strip. If the reaction pad has a blue color before applying saliva sample, do not use. 2.     Saturate the reactive pad with saliva from collection cup or by applying saliva directly to the pad. (It usually takes 6-8 seconds to be saturated.) Start timer immediately after saliva application. 3.     Read result at two (2) minutes. Compare the color of the reaction pad with the color card to determine the relative blood alcohol level.
INTENDED USE â?? A rapid animal diagnostic test kit for simple antigen detection that can diagnose the presence or absence of distemper virus antigens in dog eye secretions (eye mucus, tears), droplets, and saliva within 10 minutes with a simple operation. Symptom of a disease â?? It is a highly contagious disease. The virus spreads more widely in young dogs than in adult dogs and has a higher mortality rate. Canine distemper is a serious viral disease with no known cure, and can be transmitted from dog to dog in the air or in direct contact. Typical symptoms are respiratory and intestinal problems, such as coughing, diarrhea, vomiting, runny nose, and loss of appetite.
A one-step rapid immunochromatographic test for the quantitative detection of specific antibodies to COVID-19 present in human serum, plasma, or whole blood.
The GENEDIA W COVID-19 Ag is an in vitro diagnostic single-use test and qualitative immunoassay to detect SARS-CoV-2 antigen in nasopharyngeal swab and sputum specimen from human. This assay is designed for professional personnel in laboratory and at point-of-care as an aid in screening patients suspected of being infected and asymptomatic patients. Allow wider testing with fast test time (10 minutes) Clinically proven data of asymptomatic patients available Separately packed extraction solution to minimize the possibility of contamination No additional instruments required Package Unit : 20 Tests/Kit Expiration Date : 24 Months (while sealed in the original aluminum foil pouch) GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva The price is negotiable according to the amount of your order and shipping term. No MOQ is required but we prefer 1 pallet with 9,600 tests. (20 tests/kit, 30 kits/carton, 16 cartons/pallet)
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