Drug Addiction Rapid Tests Panel Suppliers and Manufacturers

Product Details: Number of Reactions(Preps)/Kit 10 T Brand CTK BioTech Test Type Rapid test Sample human serum, plasma, or whole blood Test time 10 Min Cat No : R0253C The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms consistent with TORCH infection. Women who are pregnant or who are planning to become pregnant Individuals with a compromised immune system The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection. The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection. The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2. Product Specification : Individually sealed foil pouches containing: One cassette device Two desiccants Plastic droppers Sample diluent (REF SB-R0253, 5 mL/bottle) One package insert (instruction for use)

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.

Corona Antigen Rapid Test Kits USD 4.85 FOB.

INTENDED USE The One Step Dengue NS1 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in serum or plasma to aid in the diagnosis of Dengue viral infection. SUMMARY Dengue is transmitted by the bite of an Aedes mosquito infected with any one of the four dengue viruses. It occurs in tropical and sub-tropical areas of the world. Symptoms appear 3 14 days after the infective bite. Dengue fever is a febrile illness that affects infants, young children and adults. Dengue haemorrhagic fever (fever, abdominal pain, vomiting, bleeding) is a potentially lethal complication, affecting mainly children. Early clinical diagnosis and careful clinical management by experienced physicians and nurses increase survival of patients. One step Dengue NS1 Ag Test is a simple, visual qualitative test that detects dengue virus NS1 antigen in human serum or plasma. The test is based on immunochromatography and can give a result within 15 minutes. 25PCS/BOX

Specification Strength/ Size Packing Size Packed In HBsAg Rapid Card Test 50 Tests 50 Box Pack

The self testing product is transformed from the professional testing product CLUNGENE COVID 19 Antigen Rapid Test manufactured by Clongene The BfArM has granted the first special approvals according to 11 paragraph 1 of the German Medical Devices Act ( of antigen tests for self administration by laypersons (self tests) for the detection of SARS CoV 2 Our self testing product can be sold and used in Germany Overview of CLUNGENE COVID 1

INTENDED USE The Helicobacter-Pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of H. pylori infection. INTRODUCTION Helicobacter pylori (also known as Campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma. The epidemiologic study shows that more than 50% of the world's population is infected by H. pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by H. pylori strains. So the detection and treatment of H. pylori strains infection is very important. At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical ELISA and immunoblot assays. This Kit belongs to non-invasive approach.

USA Manufactured, highly accurate, rapid COVID-19 Antigen test. Clinically validated by third-party medical institutions in USA and Europe (Denmark, Poland). The test is highly specific and sensitive (Specificity 100%, Sensitivity 99.1%). Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.

USA Manufactured, highly accurate, rapid COVID-19 Antibody test. Clinically validated in the USA by Harvard and UCSF Universities, and found to be best-in-class of Antibody tests. 95-100% accuracy in identifying patients after days 12. Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.

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

Introducing our Rapid Malaria Testing Kit, a breakthrough in diagnosing malaria with speed and accuracy. This cutting-edge kit is designed for easy and quick detection of the malaria parasite, revolutionizing the way healthcare professionals identify this life-threatening disease. With a user-friendly approach, it requires only a small blood sample to deliver results within minutes, enabling swift and informed medical decisions. Our kit boasts high sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact design and portability make it ideal for remote and resource-limited settings. Trust our Rapid Malaria Testing Kit for fast, dependable, and life-saving malaria diagnosis, providing critical support in the fight against this global health challenge.

Our Rapid Typhoid Testing Kit is a cutting-edge solution for swift and accurate diagnosis of typhoid fever. This advanced kit is designed for quick detection of the Salmonella Typhi bacteria, streamlining the diagnostic process for healthcare professionals. With a user-friendly approach, it requires a small blood sample and delivers results within minutes, enabling rapid treatment decisions. The kit exhibits exceptional sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact, portable design makes it ideal for remote and resource-limited areas. Trust our Rapid Typhoid Testing Kit for fast, dependable, and life-saving typhoid fever diagnosis, enhancing patient care and containment of this infectious disease.

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.

Specification Strength/ Size Packing Size Packed In HIV 1 & 2 Card Test Triline 50 Tests 50 Box Pack  

Specification Strength/ Size Packing Size Packed In Filariasis Kit Includes One test Strip, Desiccant and Dropper 50 Strip Test Per Pack 50 Box Pack

General Information One-Step HBsAb Rapid Test is to detect the Hepatitis B Virus Surface Antibody in serum, plasma or whole blood. Analytical sensitivity : 10mIU/ml-30mIU/ml of Anti-HBs Sensitivity : 99.5%, Specificity : 99.8% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min

General Information One-Step HBsAg Rapid Test is to detect the Hepatitis B Virus Surface Antigen in serum, plasma or whole blood. Analytical sensitivity : 1ng/ml of HBsAg Sensitivity :100% , Specificity : 100% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min