Cheap Drug Metabolites Rapid Test Accu-Tell® Multi-line Drug Cassette (Urine) is a rapid chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at the cut-off concentrations. TEST PROCEDURE of Saliva Rapid Test Cassette Allow the test, urine specimen, and/or controls to reach room temperature (15-30 ºC) prior to testing. 1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour. 2. Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120 �¼L) to the specimen well (S) of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below. 3. Wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10 minutes.  LIMITATIONS 1. ACCU-TELL ®  Multi-line Drug Cassette (Urine) provides only a qualitative, preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. 2. There is a possibility that technical or procedural errors, as well as interfering substances in the urine specimen may cause erroneous results. 3. Adulterants, such as bleach and/or alum, in urine specimens may produce erroneous results regardless of the analytical method used. If adulteration is suspected, the test should be repeated with another urine specimen. 4. A positive result does not indicate level or intoxication, administration route or concentration in urine. 5. A negative result may not necessarily indicate drug-free urine. Negative results can be obtained when drug is present but below the cut-off level of the test. 6. This test does not distinguish between drugs of abuse and certain medications. 7. A positive test result may be obtained from certain foods or food supplements.  We are Saliva Test Manufacturer. Note: The above information is for reference use only. Please refer to the product insert provided with the products before use.
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.
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.
Assay+ COVID-19 antigen rapid test is authorized with CE marker, the sensitivity is 90%, the specificity is 98.5%. Assay+ Covid 19 antigen rapid test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein of SARS-CoV-2 from the nasopharyngeal swab from the suspected COVID-19 patients within five days of symptom onset. This test is an aid to differentiate Covid 19 virus infection from other respiratory tract infection caused by coronavirus 229E, NL63, OC43 and HKU1, or severe acute respiratory syndrome caused by SARS-CoV and MERS-CoV. The test should be performed in moderate, high or waived complexity tests. This test can also perform for the Point of Care (POC) purpose.
Assay+ Syphilis ntibody rapid test is manufactured in Canada to detect specific syphilis IgG for the healthcare providers. Assay+ syphilis Rapid Test Kit is qualitative test device for syphilis antibodies from human serum or plasma,. This device has been OEM over one million for our customers. Sensitivity over 95% syphilis infected patients, and 100% specificity have been proved used by our customers in large quantity.
Assay+ HBV surface antigen rapid test is manufactured in Canada to detect HBV surface antigen for the healthcare providers. Assay+ HBV surface antigen Rapid Test Kit is qualitative test device for HBV antigen in human serum, plasma, whole blood. This device has been used by our end customers with large quantity. Sensitivity over 95% and 100% specificity have been proved used by our customers in large quantity.
RAPID TEST IgG/IgM - EMERGENCY RESPONSE KIT FROM THE UNITED STATES! The COVID-19 Rapid Test for Screening, Diagnosis, and Monitoring is a lateral flow immunoassay, a way to qualitatively assess the presence of IgG and IgM antibodies specific for SARS-CoV-2 from a person sample Product advantages COUNTRY OF ORIGIN The United States EARLY DISCOVERY Individual test avoids cross-infection WHOLE SPECTRUM The cover early, mid and late phase of the disease FAST RESULTS 10 minutes HIGH ACCURACY 98,43% EFFICIENCY Two types of tests on one cassette with quick result SAFETY Individual test avoids cross-infection
VivaDiag Pro SARS-CoV-2 Ag Rapid Test 396.000 pcs in stock in Prague. This is repeated every week. On order can be unlimited pieces. 25pcs in box PRICE DEPEND ON QUANTITY IN ALL CASE WE CAN MAKE BEST PRICE FOR YOU. CE 1434 REF VCD16-01-011 Manual IFU ENG, DE, PORTUGAL, FRANCE, CZECH, GREECE, ITALIAN Photos, documents and video can be sent. Please contact me.
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)
Rapid antigen test kits.
Rapid antigen test kits.
Uncut sheet ag rapid test.
Rapid test kits.
Rapid antigen test kits.
Accu chek active test strips.
Antibody And Antigen Test Kits.
