Find Verified Rapid Test Kits Suppliers, Manufacturers and Wholesalers

Model:FCY-ATG01-SA
SARS-CoV-2 Antigen Test kit
Saliva
Rapid test by Mouth: 15minutes

Certificates: CE, ISO13485

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.

The H pylori can be utilized as a rapid screening process for large populations of patients and highly indicated in the early diagnosis of H pylori infection as the immune response can often precede clinical manifestations of disease From a diagnostic point of view, a high serum level specific antibodies against H pylori must be interpreted as an indication of type B asymptomatic gastritis

Specification:
Specimen:Serum/plasma/whole blood
Sensitivity:96%
Specificity:90%
Packaging:25 cassettes/box,
Certificate:CE and ISO 13485
Raw materials is imported from US
OEM packaging is available

2019-nCoV Neutralizing Antibody Test Kit
Fluorescence Immunochromatography
(Serum/plasma)

Rapid Test: Just for 15 Minutes
Accurate Result: Fluorescence immunoassay, high sensitivity
Convenient operation with smart POCT analyzers
Rate COVID-19 Vaccine immediately

Application
By testing neutralizing antibody titer after COVID-19 Vaccination,
it will be able to figure out the vaccine efficiency

Product Information
Product Name: 2019-nCoV Neutralizing Antibody Determination Kit
Methodology:Fluorescence immunoassay
Size:25 Tests/box
Storage and Validity:Stored at 2-30 within 18 months
Specimen:-Clinical fresh human serum, recommended EDTA anticoagulant plasma

Easy Operation:
1 Take 100 sample to buffer and mix 5-10s
2 Add 80 mixed sample to strip
3 Incubation time: 15 mins
4 Put strip into analyzer to test

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#Antigen rapid test kit #anti-epidemic
Provide high-quality products at competitive prices
Product: SARS-CoV-2 Antigen Rapid Test Kit
Standard: CE, FDA certification
Packing quantity: 25tests/box
FOB: US$1.60/test

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Antibody rapid test kits:
Our test kits are superior in sensitivity and specificity. All have CE and FDA registration. Now we are able to offer these same goods and services to your establishment.
Delivery 14 days.
If you are interested, please do not hesitate to contact us.
Thank you for your kind attention.
Best regards.
Chaveng Munchantip (George)
Director (Medical Supplies)

Antibody rapid test kits:
Our test kits are also superior in sensitivity and specificity. All have CE and FDA registration. Now we are able to offer these same goods and services to your establishment.

Delivery 14 days.

If you are interested, please do not hesitate to contact us.

Thank you for your kind attention.

Best regards.

Chaveng Munchantip (George)
Director (Medical Supplies)

GraceTree COVID-19 IgM/IgG
Rapid differential detection kit for IgM and IgG against COVID-19 in human serum, plasma and whole blood

Feature & Type : IgM/IgG
1) COVID-19 IgM/IgG : blood test
2) Dual-band results for simple interpretation
3) Multivariable analysis of immunoglobin IgG & IgM
4) Positive percent agreement (PPA) = 96.0%
Negative percent agreement (NPA) = 98.99%
5) Room temperature storage ( 2~30C / 36~86F )
6) Time to result : 2 min
7) Expiration date of this kit is 6 months after its manufacture date
8) MATERIALS PROVIDED
- Test device individually foil-pouched with a desiccant
- Assay solution in dropping bottle
- Capillary tube for sample loading
- Instructions for Use
- Packing: 1 box of 25 Test units
- Product Origin : South Korea
- Certificate : FDA EUA Certificate will be proved near 15. September. 2020
- Shipping Terms : FOB
- Payment Terms : T/T
- MOQ : Under Discussion
- Contract : Direct contract seller / Depending on volume, direct contract with a subsidiary of seller which is listed on stock market(in S.Korea)
- LOI, POF needed for seller

KOSTEC can supply Korean rapid test kits, which are not only faster and easier in test but alsoprovide accurater test results. Also price is very much attractive! If you have any interest in this test kits, do not hesitate to contact me. Thanks!