Produse pentru testează (162)

The Dengue NS1 Rapid Cassette Test (Whole Blood/Serum/Plasma) is a rapid immunochromatographic test for the qualitative detection of Dengue virus NS1 antigen in human whole blood, serum or plasma, as an aid in the diagnosis of Dengue infections. . widely distributed in tropical and subtropical areas of the world, causing up to 100 million infections per year.2 Classic Dengue infection is characterized by sudden onset of fever, intense headache, myalgia, arthralgia and rash cutaneous. NS1 is one of the 7 non-structural proteins of the Dengue Virus believed to be involved in viral replication. NS1 exists as a monomer in its immature form but is rapidly processed in the endoplasmic reticulum to form a stable dimer. A small amount of NS1 remains associated with intracellular organelles where it is thought to be involved in viral replication. The remainder of NS1 is found associated with the plasma membrane or is secreted as a soluble hexadimer. Product code:SC-0548-25

Multi Drug Rapid Test Panel – Product Code: SC-2092-25 Drug Test in the well version that analyzes Cocaine, Marijuana, Amphetamines. Morphine, Opiates, Benzodiazepines. Analyzes: AMP 300, MET 300, THC 30, COC 300, MDMA 300, MOP 300. This Drug Test has a result printing system through its software tool, or the test result can also be read visually. The instrument automatically reads and interprets the result of the test with alpha numeric reading, bringing it back to a file to be printed (Objective Print of the Result). (The 120ml urine container is supplied separately, you can buy it on the “Accessories” page). Product code:SC-2092-25

ScreenVet LSH antibody rapid cassette test (whole blood/serum/plasma) is based on the principle of lateral flow immunochromatographic examination and uses the direct flow method for the qualitative detection of Leishmania antibody (LSH Ab) in whole blood, serum or canine plasma. The Leishmania ScreenVet Test Kit is designed to detect Leishmania antibodies in whole blood, serum or plasma. After being absorbed by the cellulose swab, the Leishmania antibodies move and bind to the Leishmania antigen orocolloid complex on the conjugated swab, forming an Ag-Ab complex. This complex then forms an Ag-Ab-Ag sandwich directly linked to the Leishmania antigen (Ag) on ​​the nitrocellulose membrane. The test results can form the Control and Test lines for which the principles of immunochromatography are employed. Product code:SCV-1125-10

Sars-Cov-2 Rbd-Igg Rapid Test – Product code: SC-1415-20 COVID-19 IgG Rapid Test Cassette (Whole Blood/Serum/Plasma) is a lateral flow immunochromatographic assay for the qualitative detection of IgG antibodies that bind to the receptor binding domain (RBD) of the SARS-Cov-2 spike (S) and / or Nucleocapsid (N) protein in whole blood, serum or plasma specimens. The COVID-19 IgG rapid test (Whole Blood/Serum/Plasma) is intended for use as an aid in the identification of individuals with an adaptive immune response to SARS-CoV-2. False positive results are possible due to cross-reactivity of pre-existing antibodies or other possible causes. Due to the risk of false positive results, confirmation of positive results by another IgG test of a different nature should be considered. The new coronavirus (SARS-CoV.2) belongs to the β genus. COVID-19 is an acute respiratory infectious disease. Product code:SC-1415-20

The rapid Screen Test Igg Sars-Cov-2 S-RBD test from whole prick blood is a rapid immunochromatographic test for the qualitative detection of IgG antibodies to the receptor binding domain (RBD) spike (S) protein of SARS-CoV-2 in human whole prick blood at approximately 10 days after vaccination. Screen Test Covid-19 Igg Sars-Cov-2 S-RBD is an in vitro diagnostic medical device CE 1434. Read the warnings and operating instructions carefully. PHARMACIST CODE:983834096

FIV Antibody + FeLV Antigen Combo (Whole Blood/Serum/Plasma) is a combined rapid cassette test, capable of separately diagnosing the presence of Feline Immunodeficiency Antibody and Feline Leukemia Virus Antigen in Feline Whole Blood, serum or plasma. FIV Antibody + FeLV Antigen Combo is a lateral flow immunochromatographic rapid cassette test using the direct (or Sandwich) method. The device has two test windows. Each test window has an invisible T (test) zone and C (control) zone. When the sample is applied to the wells (S) on the cassette, the liquid flows sideways on the surface of the test strip. If there is a sufficient amount of Feline immunodeficiency antibody or Feline leukemia virus antigen in the sample, a visible T line will be displayed in the corresponding test window. Line C should always appear after applying a sample, thus indicating that the result is valid. Product code:SCV-1101-10

The Clostridium difficile Toxin A + Toxin B combination rapid test (Feces) is a rapid chromatographic immunoassay for the qualitative detection of Toxin A and Toxin B Clostridium difficile antigens in human stool samples. The Clostridium difficile Toxin A + Toxin B Combination Rapid Test detects two distinct antigens in stool samples for C. difficile, viz., Toxin A and Toxin B on two different test strips in the same device, thus simultaneously detects two specific Clostridium antigens hard. Clostridium difficile is an anaerobic bacterium that acts as an opportunistic pathogen: it grows in the intestine when the normal flora is altered by antibiotic therapy. Toxigenic strains of Clostridium difficile cause infections from simple diarrhea to pseudomembranous colitis, which can even cause death. The disease is caused by two toxins produced by the toxigenic strains of C. difficile: Product code:SC-0494-10

Screen Test Vitamin D is a rapid test for self-diagnostic use to detect the amount of vitamin D in human blood. For in vitro self-diagnostic use only. This test can provide a preliminary diagnostic result and can be used in screening for vitamin D deficiency. Screen Check Test Vitamin D is an in vitro diagnostic medical device CE 0123. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:970791758

Chikungunya Igg/Igm Rapid Test – Product code: SC-0517-20 The Chikungunya IgG/IgM rapid test (Whole Blood/Serum/Plasma) is a rapid immunoassay for the detection of IgG and IgM antibodies to Chikungunya in human whole blood, serum or plasma. It is meant to be used as a screening test and as an aid in diagnosing CHIK infection. Chikungunya is a viral infection transmitted by the bite of an infected Aedes aegypti mosquito. It is characterized by irritation, fever, and severe joint pain (arthralgia) that usually last three to seven days. Chikungunya is a viral infection transmitted by the bite of an infected Aedes aegypti mosquito. It is characterized by irritation, fever, and severe joint pain (arthralgia) that usually last three to seven days. The name derives from a word Makonde which means “the one who bends” in reference to the bent posture that develops as a result of the painful arthritic symptoms caused by the disease. Product code:SC-0517-20

Sars-Cov-2 Igg/Igm Rapid Test – Product code: SC-1200-10 Rapid Covid 19 Serological Test for the qualitative detection of IgG and IgM antibodies to 2019-nCov, Sars-CoV-2, Coronavirus virus in human whole blood, serum or plasma samples. For professional in vitro diagnostic use only. The Covid-19 IgG/IgM Screen Test Rapid Serological Test (2019-nCOV), (Sars-CoV-2), is a lateral flow chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies. The new coronaviruses belong to the β strain. COVID-19 is an acute respiratory infectious disease. The population is generally susceptible to it. From what has been observed so far, the main source of new infections are coronavirus infected patients; even infected people without symptoms can be a source of infection. According to current epidemiological investigations, the incubation period is 1-14 days, mostly between 3 and 7 days. The main symptoms include fever, fatigue and dry cough. Product code:SC-1200-10

Tetanus Rapid Test – Product code: SC-0746-40 Rapid immunoassay for the qualitative detection of tetanus toxin antibodies in whole blood, serum or plasma to aid in the diagnosis of tetanus toxin infection. The test is designed to assist in the tetanus prophylaxis of patients at risk. Since this disease does not confer immunity, the only prevention is vaccination. Immunoprotection is given by measuring the concentration of tetanus antibodies. As part of emergency medicine, knowing in real time the immune status of subjects at risk (deep wounds) allows for better management of appropriate tetanus prophylaxis. Clostridium tetani is a bacterium that causes tetanus in humans. Clostridium tetani are gram-positive spore-forming rods that are anaerobic. If they enter the body through a wound, they can multiply and produce a toxin that affects the nerves and controls muscle activity. Clostridium tetani toxin binds to peripheral nerve cell membranes and inhibits the release of neurotransmitters. Product code:SC-0746-40

Malaria P.F./P.V. Rapid Test – Product code: SC-0661-25 The Malaria P.f./P.v. (Whole Blood) is a rapid chromatographic immunoassay for the qualitative identification of two types of Plasmodium circulating in whole blood: falciparum (P.f.) and vivax (P.v.). The Malaria P.f./P.v. (Whole Blood) is a qualitative, membrane-based immunoassay for the detection of P.f. and P.v. in whole blood. The membrane is pre-coated with anti-HRP-II and anti-pLDH antibodies. During testing, the whole blood sample reacts with the colored conjugate with which the test media was pre-coated. The compound then migrates upward on the membrane by capillary action and reacts with anti-Histidine Rich Protein II (HRP-II) antibodies on the membrane in the test line area P.f. and with anti-pLDH antibodies in the P.v test line region. If the sample contains Plasmodium-specific HRP-II or P. vivaxLDH or both, a colored line appears in the P-f- or P.v test line region. or both. Product code:SC-0661-25

Sars-Cov-2 Antigen Oral Fluid Rapid Test – Product code: SC-1286-20 The Covid-19 Antigen Rapid Test Cassette (Oral Fluid) is a rapid chromatographic immunoassay test for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens in oral fluid samples from individuals with suspected SARS-CoV-2 infection in combination with the clinical presentation and the results of other laboratory tests. The results are for the detection of SARS CoV-2 nucleocapsid protein antigens. During the acute phase of infection, an antigen is usually detectable in upper respiratory tract samples. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is required to determine the status of the infection. Positive results do not rule out bacterial infection or coinfection with other viruses. The agent identified may not be the definitive cause of the disease. Product code:SC-1286-20

Quickly measures blood pressure and heart rate. Through a cuff attached to the instrument and placed around the forearm, diastolic and systolic blood pressure can be monitored. Screen Check Test Blood Pressure Monitor is a CE 0482 Medical Device. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:970791796

The Giardia ScreenVet test is designed to detect Giardia Iamblia antigens in stool. Two antibodies in the kit specifically bind to different epitopes of the antigens. After being absorbed by the cellulose pad, the Giardia Iamblia antigens move and bind with the anti-Giardia oro-colloidal complex on the conjugate pad, forming an Ab-Ag complex. This complex then forms an Ab-Ag-Ab sandwich by binding directly with the antibody of another monoclonal anti-Giardia in the nitrocellulose membrane. The test results can appear on the Control and Test lines that employ the principles of immunocromatography. Product code:SCV-1088-10

Rapid test for qualitative detection of protein nucleocapsid SARS-CoV-2 and nucleoprotein antigens of influenza A and influenza B present in the nasal swab sample. The Rapid COVID-19 and Influenza A + B Antigen Test (nasal swab) is a membrane-based qualitative immunoassay for the determination of SARS-CoV-2 and Influenza A + B antigens from a swab of human nasal sample. Result in 15 minutes. Screen Test Sars-Cov-2 + Influenza A + B is an in vitro diagnostic Medical Device CE 1434. Read the warnings and operating instructions carefully. PHARMACIST CODE:984818930

Syphilis Rapid Test – Product code: SC-0722-40 Rapid test for the diagnosis of Syphilis to qualitatively detect antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma. The Syphilis Rapid Test (Whole Blood / Serum / Plasma) is a qualitative, membrane-based immunoassay for the detection of TP antibodies (IgG and IgM) in whole blood, serum or plasma. In the procedure of this test, a recombinant Syphilis antigen is immobilized in the area of ​​the test line. After the sample is poured into the well of the holder, it reacts with the Syphilis antigen coated particles in the test. This compound then migrates upwards on the membrane chromatographically and reacts with the immobilized Syphilis antigen. The dual antigen test format can detect both IgG and IgM in samples. If the sample contains TP antibodies, a colored line will appear in the test area indicating a positive result. Product code:SC-0722-40

Coronavirus Ag Test (Feces) is an immunochromatographic test for the qualitative detection of feline coronavirus antigen (FCoV Ag) in feline feces. The test cassette has a test window. The test window has a T (test) zone and a C (control) zone. When the sample is applied in the sample well on the cassette, the liquid flows laterally on the surface of the test strip. If sufficient feline coronavirus antigen is present in the sample, a visible T-line will appear. Line C should always appear after a sample is applied, indicating a valid result. In this way, the cassette can accurately indicate the presence of feline coronavirus antigen in the sample. Free-sale product not intended for medical purposes. PHARMACIST CODE:984845418

Influenza A+B Rapid Test – Product code: SC-0623-20 Rapid test for the qualitative detection of the Influenza A and Influenza B virus on samples of nasal swab, throat swab or nasal aspirate. The Influenza A + B rapid test is a rapid immunochromatographic test for the qualitative identification of influenza A and B antigens on nasal, pharyngeal or nasal aspirate swab samples. It is intended to assist in the rapid differential diagnosis of viral infections of influenza A and B. Influenza is an acute, highly contagious viral infection of the respiratory tract. It is a highly transmissible contagious disease through coughing and sneezing from suspended droplets containing the live virus. The peak of the flu usually occurs during the winter and autumn months each year. Type A viruses are usually more prevalent than type B and associated with more serious influenza outbreaks, while type B infections are usually milder. Product code:SC-0623-20

Created as a Reader for the Objective Printing of the Drug Test for Occupational Medicine, it was then adapted to the reading of other tests as well. Tool for the Objective Printing of the drug test created for the Occupational Medicine Law, notified to the Ministry of Health. The system consists of the Screen Reader Software plus Screen Box Reader and is able to read drug tests giving alphanumeric reading results, the tool allows you to carry out the Objective Print of the Drug Test Result with reading of the Creatinine and Ph. Our Screen Reader software can be installed on multiple computers, it has a license cost of €70 starting from the second year. It works with Windows XP, Windows Vista, Windows 7, Windows 8 and Windows 10. PRODUCT CODE:SC-1194-01

Screen Pregnancy Test is a rapid test for self-diagnostic use that detects possible pregnancy in 3 minutes. Rapid test to check pregnancy status. Screen Mamma Pregnancy Test is an in vitro diagnostic Medical Device CE 0373. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:912359270

Multi Line Drug Rapid Test Cassette – Product code: SC-0111-25 Drug Test through urine that detects 5 substances simultaneously with specific result for each substance analyzed. The test analyzes: Oxycodone, EDDP, Phencyclidine Tramadol, K2 Synthetic Marijuana. (OXY / EDDP / PCP / TML / K2). (The 120ml urine container is supplied separately, you can buy it on the “Accessories” page). Product code:SC-0111-25

Sars-Cov-2 Antigen Rapid Test – Product code: SC-1255-20 The Covid-19 rapid antigen test is a rapid immunochromatographic nasopharyngeal swab for the qualitative detection of Sars-CoV-2 antigens present in the human nasopharynx. For professional in vitro diagnostic use only. The Covid-19 Rapid Antigen Test (Nasopharyngeal swab) is a rapid immunochromatographic test for the qualitative detection of Sars-CoV-2 antigens present in nasopharyngeal swab samples. The results detect Sars-CoV-2 antigen. The antigen is generally found in swabs of the upper respiratory tract during the acute phase of the infection. Positive results indicate the presence of viral antigens, but a clinical correlation with the patient’s medical history and other diagnostic information is required to determine the infectious state. The positive results do not exclude bacterial infection or co-infections with other viruses. s. Product code:SC-1255-20

The SARS-CoV-2 (COVID-19) Antigen Rapid Test (Saliva) is a single-use test intended to detect in human saliva the novel coronavirus SARS-CoV-2 that causes COVID-19. This test is designed for home use with saliva samples collected independently from symptomatic individuals suspected of being infected with SARS-CoV-2. With the rapid SARS-CoV-2 (COVID-19) antigen test (Saliva), only a preliminary result is obtained; final confirmation should be based on the results of clinical diagnosis. Result in 15 minutes. Screen Check Test Covid-19 Saliva is an in vitro diagnostic medical device CE 1434. Read the warnings and instructions for use carefully. PHARMACIST CODE:984818942

Multi Line Drug Rapid Test Cassette – Product code: SC-0258-25 Drug test that detects 10 substances in urine: Cocaine and metabolites (300), Amphetamines (500), Methamphetamines (500), Ecstasy MDMA (500), Marijuana (Cannabinoids THC) (50), Opiates (Morphine, Heroin and metabolites) (300), Benzodiazepines (300), Methadone (300), Buprenorphine (10), TCA Antidepressant tricycles (1000). (The 120ml urine container is supplied separately, you can buy it on the “Accessories” page). Product code:SC-0258-25

Sars-Cov-2 Antigen + Flu A/B Rapid Test – Codice Prodotto: SC-1262-20 The Covid-19 Antigen Rapid Swab and Influenza A + B (nasopharyngeal swab) is a rapid immunochromatographic test for the qualitative detection of the antigens of the Sars-CoV-2, Influenza A and Influenza B viruses present in the human nasopharynx. For professional in vitro diagnostic use only. The separate results indicate the detection of Sars-CoV-2 and Influenza A + B antigens. The antigen is generally detectable in upper respiratory tract samples during the acute phase of the infection. Positive results indicate the presence of viral antigens, but a clinical correlation with the patient’s medical history and other diagnostic information is required to determine the infectious state. The positive results do not exclude bacterial infection or co-infections with other viruses. Product code:SC-1262-20

Screen Test Stool Blood is a rapid test for self-diagnostic use that detects the presence of occult human blood in stool. Test Fob. Screen Check Stool Blood Test is an in vitro diagnostic Medical Device CE 0123. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:912359268

Screen pregnancy test, rapid test for self-diagnostic use that detects possible pregnancy in 3 minutes. Pack of 2 pieces. Rapid test to check pregnancy status. Screen Mum Pregnancy Test is an in vitro diagnostic Medical Device CE 0373. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:912359231

Screen Test Influenza A/B is a rapid qualitative test for self-diagnostic use that can detect influenza type A (including H1N1) and type B nucleoprotein antigen by extraction of a nasal swab or pharyngeal swab. The product serves as an aid in determining infection to influenza type A and B viruses. Screen Check Test Influenza A/B is an in vitro diagnostic Medical Device CE 0123. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:922411739

Multi Line Drug Rapid Test Cassette – Product code: SC-0241-25 Drug test that detects 10 substances in urine: Cocaine and metabolites (300), Amphetamines (1000), Meth-Amphetamines (1000), Ecstasy MDMA (500), Marijuana (Cannabinoids THC) (50), Opiates (Morphine, Heroin and metabolites) (300), Benzodiazepines (300), Methadone (300), Pencyclidine (25), Barbiturates (300). (The 120ml urine container is supplied separately, you can buy it on the “Accessories” page). Product code:SC-0241-25