The Accu-Chek Performa Test Strips are used in conjunction with Accu-Chek Performa blood glucose meters. These test strips are an essential component for monitoring blood glucose levels in individuals with diabetes. Here are some key points about Accu-Chek Performa Test Strips:
Compatibility: Accu-Chek Performa Test Strips are specifically designed to work with Accu-Chek Performa blood glucose meters.
Blood Glucose Monitoring: These test strips are used to measure the concentration of glucose in a small blood sample. This helps individuals with diabetes manage their blood sugar levels.
Quick Results: The test strips provide rapid and accurate results, allowing individuals to monitor their blood glucose levels conveniently at home.
Capillary Action Technology: The strips often use capillary action technology, which helps to draw in a precise amount of blood for the test.
Coding: Some blood glucose test strips require manual coding to match the code on the test strip vial with the code on the meter. It's important to follow the specific instructions provided by the manufacturer regarding coding.
Storage: Proper storage of test strips is essential for accurate results. Test strips are typically stored in a cool, dry place, and users should check the expiration date before use.
Accu-Chek test strips are essential components of blood glucose monitoring for individuals with diabetes. These strips are designed to work seamlessly with Accu-Chek blood glucose meters, enabling accurate and reliable measurement of blood sugar levels. The strips utilize advanced technology to require only a small blood sample, making the testing process more comfortable. With rapid and precise results, Accu-Chek test strips empower users to effectively manage their diabetes by providing valuable insights into their current glucose levels. This user-friendly and indispensable tool plays a crucial role in facilitating proactive health management for individuals living with diabetes.
Product Name Specimen Catalog No. Quantity per box
Alcohol Strip Saliva ABT-ACH-A187 100T/50T
KEY POINTS
Detection for: Â Alcohol in human saliva at a cut-off concentration of 0.02% (20mg/dL);
Reading time: Â 2 minutes;
Agreement: Â 98%.
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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.
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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.
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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. Â Â Â Â 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. Â Â Â Â 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. Â Â Â Â Read result at two (2) minutes. Compare the color of the reaction pad with the color card to determine the relative blood alcohol level.
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. Â Discard the collector. Â 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.
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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: Â Ehyl alcohol in human urine greater than 0.04%(40mg/dL);
Reading time: Â 3 minutes;
Relative Sensitivity: Â 96%;
Relative Specificity: Â 100%;
Agreement: Â 98%.
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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.
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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.
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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.
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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. Â Discard the collector. Â 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.
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Progesterone (P4) is a kind of steroid hormone. The concentration change of P4 in milk is one specific characteristic indicating the activities of cow ovary. It plays an important role in the process of maternal reproduction and maintaining pregnancy.
Therefore, it can be monitoring cow reproductive activity by detecting the concentration of P4. P4 concentration has different characteristic changes as the cow's stage of reproductive physiology, through to detect the progesterone levels can make an accurate diagnosis of cow in early pregnancy.
PRODUCT FEATURES
The strip can be used for diagnosis of cow early pregnancy, which is of high accuracy, easy operation, rapid and normal temperature storage, easy to carry, harmless to maternal and fetal safety.
THE SCOPE OF USE
The test is mainly suitable for dairy and beef cattle early pregnancy diagnosis, as well as to guide timely artificial insemination.
THE BEST USE DATE
Cow's estrus cycle is 21 days. There are individual differences in 18 to 24 days commonly, it is suggested to perform the test the 18th days after mating. Perform the test once every day for 5 continuous days; even if one negative result appears during the five days, which indicates the cow is not pregnant and P4 is at the lowest level at this moment. In this case, it was suggested to have the dairy cow mated in time; that should improve the conception rate. If positive results show for all 5 days tests, it indicates the cow is in pregnancy, and it should get careful nursing and gestation management. Another test method is to closely observe the cow rutting performance from 18 days after mating, if it was in rutting performance the detection should do immediately; for those that have no heat after mating to do a test on the 24th day.
SPECIMEN COLLECTION
1.Milk sample: cleaning teats before take the milk, abandon to the first three milk, then collect milk in the bottle, take 1 ml in the test tube, placed the centrifuge10000 rpm for 10 minutes, in vitro milk sample was divided into three layers, using straws inserted in the underlying absorbing liquid cream and set aside.
2.Saliva: from the mouth collecting saliva for 3 to 5 ml placed the centrifuge 1500-2000 rpm for 5 minutes, take supernatant on standby.
3.The galley proof: from the hair root galley proof according to take 10 mg in the extracting pipe, add 3 ml anhydrous ethanol soak vortex shock 5 minutes after 2-3 hours, placed 3000 rpm centrifuge for 5 minutes, drain on ethanol solution 1 ml into glass dish, in 70-80 �?? oven dry reoccupy after 1 ml PBS dilution. Set aside.
4.Urine: can be used directly.
5.Blood: anticoagulant take 1 to 2 ml of centrifugal 2000 rpm 5-10 minutes from the plasma standby, the anticoagulant let stand for 30 minutes to separate serum blood clots. Set aside.
COVID-19 IgG IgM and Influenza A&B antigen Sealing Tube Test Strip Colloidal Gold
INTENDED USE
Amazing COVID-19 Ag/Ab IgG/IgM and Influenza Ag AB Sealing Tube Twin Test Strip is a lateral flow immunochromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 and Influenza virus.
The kit has two strips. One is for the qualitative detection of COVID-19 nucleocapsid protein antigen and Influenza virus type A in human nasopharyngeal, nasal secretion, saliva or and serum directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Another is for the qualitative detection of COVID-19 antibody IgG/IgM in human serum, plasma sodium citrate, sodium heparin, dipotassium EDTA and whole blood sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood and Influenza virus type B in human nasopharyngeal, nasal secretion, saliva or/and serum specimens to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests.
PRINCIPLE
There are two test strips in the Amazing COVID-19 Antigen IgG IgM Filmseal Tube Twin Test.
COVID-19 antigen test strip is based on sandwich lateral flow immunochromatographic assay highly sensitively detecting COVID-19 nucleocapsid protein in human nasopharyngeal, nasal secretion, saliva or and serum specimens, having an invisible T test zone and C control zone. When the sample is applied into the test tube, the liquid will laterally flow on the surface of the test strip. If there is enough COVID-19 antigen in the sample, a visible T band will appear.
COVID-19 IgGIgM test strip is based on lateral flow immunochromatographic assay highly sensitively detecting COVID-19 IgG and IgM in human whole blood, serum, or plasma specimens, having an invisible IgGT1 zone, IgMT2 zone, and C control zone. When the sample is applied into the test tube, the liquid will laterally flow on the surface of the test strip. If there is enough COVID-19 IgG or and IgM in the sample, a visible IgGT1 or and IgMT2 band will appear in the corresponding area. The C band of two strips should always appear after a sample is applied, indicating a valid result. By this means, the kit can accurately indicate the presence of COVID-19 antigen, IgG, and IgM in the sample.
Our New Precision Saliva Drug Test is an inexpensive screening test for the simultaneous detection of drugs in human saliva. Custom configurations are available on all rapid drug test products.
Features
CE Mark, Health Canada II & III
99% accuracy, USA Made strips and reagents
Immediate Rapid Results: Read Negatives within 1 minute, positive in 5 minutes
Simple Swab, insert, and read results
Easy to read strips with definitive lines
Swab stem color indicator ensures optimal saliva saturation/collected.
25+ Drug Test options
24 Month Shelf Life from Date of manufacture
Results Stable for 30 Hour
OEM & Private Label available
Call for volume discounts!
Benefits
Same Money & Quality Product
Superior Personal Service
Available after regular business hours
Free Online Training, Product Certification, Product Training Video
Free Lab LC-MS/MS set up, free overnight shipping, air bills, boxes, lab packs, specimen bags
These are screening devices read positive or negative, qualitative, and accurate, if you read positive, we recommend a certified lab for LC-MS/MS Confirmation.
These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
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.
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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.
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Note: The above information is for reference use only. Please refer to the product insert provided with the products before use.
COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Test Strip (Colloidal Gold):-
INTENDED USE:
Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip is a lateral flow immunochromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 and Influenza virus.
The kit has two strips. One is for the qualitative detection of COVID-19 nucleocapsid protein antigen and Influenza virus type A in human nasopharyngeal, nasal secretion, saliva or/and serum directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Another is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA) and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) and Influenza virus type B in human nasopharyngeal, nasal secretion, saliva or/and serum specimens to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests.
Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
COVID-19 Ag/Ab Sealing Tube Twin Test Strip (Colloidal Gold)
INTENDED USE:
Amazing COVID-19 Ag/Ab Sealing Tube Twin Test Strip is a lateral flow immuno- chromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 nucleocapsid protein antigen and COVID-19 antibody (IgG/IgM). The kit has two strips. One strip is for the qualitative detection of COVID-19 nucleocapsid protein antigen in human nasopharyngeal, nasal secretion, saliva or/and serum specimens directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Another strip is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA), and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests. Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
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