Produse pentru ecran (198)

Screen Test Menopause is a rapid test for self-diagnostic use detects the presence of FSH Hormone, can help determine if a woman is in the perimenopausal phase. The package contains 2 tests. Menopause is the permanent cessation of menstruation. The period leading to menopause and the 12 months following are known as perimenopause. Discomfort such as sleep disturbances, vaginal dryness, hair loss, anxiety and mood swings, short-term memory loss, and exhaustion may occur during this period. Screen Check Test Menopause is an in vitro diagnostic Medical Device CE 0123. Read the warnings and operating instructions carefully. Authorization of 7/04/2021. PHARMACIST CODE:912359256

Sars-Cov-2 Neutralization Antibody Rapid Test – Product code: SC-1569-20 The SARS-CoV-2 Neutralizing Antibody Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid immunochromatographic test designed for the qualitative detection of neutralizing antibodies against SARS-CoV-2 that block the interaction between the domain that binds the viral spike glycoprotein receptor (RBD) and cell surface receptor ACE2 in human serum, plasma or whole blood. It is intended to be used as an aid in the identification of individuals with an adaptive immune response to SARS-CoV-2. This test should not be used to diagnose acute SARS-CoV-2 infection. The results indicate the detection of neutralizing SARS-CoV-2 antibodies. Positive results indicate the presence of neutralizing SARS-CoV-2 antibodies. The new coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. Product code:SC-1569-20

Mycoplasma Pneumoniae Antigen Test – Product code: SC-0654-25 Rapid test for the qualitative detection of Mycoplasma Pneumoniae Antigen on a pharyngeal sample. For professional in vitro diagnostic use only. The rapid test for Mycoplasma Pneumoniae Antigen is a rapid chromatographic immunoassay for the qualitative detection of mycoplasma pneumoniae (M. Pneumoniae) antigens in human throat swabs. It is intended to assist in the rapid differential diagnosis of mycoplasma pneumoniae infections. M. pneumoniae is one of three Mycoplasma species that frequently cause infections in humans. M. pneumoniae most commonly causes upper respiratory tract infections, but it can also cause pneumonia. The identification of M.pneumoniae will help in the treatment of the disease with appropriate antibiotic therapy. This immunoassay for M. pneumoniae is designed to qualitatively detect the M. pneumoniae antigen. Product code:SC-0654-25

AS can be equipped with slotted or holed baskets. Special rotor has been foreseen to ensure low pulsation.

Part of the stock is conveyed to DSC and its function is doing a stock pre screening and keeping, as much as possible, pulper’s vat clean.

Mycoplasma Pneumoniae IgG/IgM Rapid Test – Product code: IMP-425 A rapid test for the qualitative detection of IgG and IgM antibodies to Mycoplasma pneumoniae (M. pneumonia) in whole blood, serum or plasma. The Mycoplasma pneumoniae IgG/IgM Combo Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Mycoplasma pneumoniae in whole blood, serum, or plasma to aid in the diagnosis of Mycoplasma pneumoniae infection. Mycoplasma pneumoniae is the causative agent of respiratory tract nfectious diseases and complication of other systems. There will be a symptom with headache, fever, dry cough, and muscle pain. People of all age groups can be infected while youth, middle-aged and children under 4 years old have a higher infection rate. 30% of the infected population may have a whole lung infection. Product code:IMP-425

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

Hbsag Rapid Test – Product code: IHBSG-402 Rapid test for the qualitative detection of Hepatitis B surface antigen (HbsAg) in whole blood, serum or plasma. The Hepatitis B – HBsAg Cassette Rapid Test Cassette is a rapid test for the qualitative detection of the presence of HBsAg in whole blood, serum or plasma samples. The test uses a combination of monoclonal and polyclonal antibodies to selectively detect high levels of HBsAg in whole blood, serum or plasma. Viral hepatitis is a systemic disease that primarily involves the liver. Most cases of acute viral hepatitis are caused by hepatitis A virus, hepatitis B virus (HBV) or hepatitis C virus. The complex antigen found on the surface of HBV is called HbsAg. Previous designations include the Australia or Au antigen.1 The presence of HBsAg in whole blood, serum or plasma indicates both acute and chronic active hepatitis B infection. Product code:IHBSG-402

Lyme IGG/IGM Rapid Test – Product code: ILY-402 Rapid test for the qualitative detection of anti-Borrelia IgG and IgM antibodies in human whole blood, serum or plasma samples. For professional in vitro diagnostic use only. Screen Test Lyme IgG/IgM is a lateral flow immunochromatographic test for the qualitative detection of anti-Borrelia IgG and IgM antibodies in human whole blood, serum or plasma samples. Lyme disease, also known as Lyme borreliosis, is an infectious disease caused by bacteria of the genus Borrelia sp. which is spread by ticks. The most common sign of infection is an expanding red area on the skin, known as erythema migrans, that begins at the site of the tick bite about a week after it occurs. The rash is typically neither itchy nor painful. About 25 to 50 percent of infected people do not develop a rash. Other early symptoms may include fever, headache and feeling tired. Product code:ILY-402

Hav Igm Rapid Test – Product code: SC-0562-25 Rapid test for the qualitative detection of the hepatitis A virus on serum or plasma. For professional in vitro diagnostic use only. The HAV IgM test on cassette is a rapid chromatographic immunoassay for the qualitative detection of IgM antibodies to the hepatitis A virus (HAV) in serum or plasma. The HAV IgM rapid test cassette was created to detect anti-HAV IgM in less than 20 minutes by not necessarily qualified medical personnel and without bulky laboratory equipment. HAV is a positive RNA virus, a unique member of picornavirdae1. Its transmission depends mainly on serial transmission from person to person via fecal gold. Although hepatitis A is not normally a sexually transmitted disease, the infection rate is high among male homosexuals, due to oral-anal contact. The HAV IgM Rapid Test should be used to detect anti-HAV IgM in less than 15 minutes even by untrained or unskilled personnel, without bulky laboratory equipment. Product code:SC-0562-25

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

Norovirus Rapid Test – Product code: SC-0678-25 The rapid test for Norovirus (Feces) is a rapid immunochromatographic test for the qualitative detection of Norovirus in human stool samples useful in the diagnosis of Norovirus infection. The Norovirus rapid test (Feces) was compared with the RT-PCR method, demonstrating an overall accuracy of 94.29%. The presence of a colored line in the T1 area indicates a positive result for Genogroup 1 while in T2 it indicates a positive result for Genogroup 2, while its absence indicates a negative result. As a procedural control, a line will always appear in the control region (C) to indicate that the correct volume of sample has been used and that the membrane has been soaked. Noroviruses (NoVs) are a genetically diverse group of single-stranded RNA viruses, belonging to the Caliciviridae family. Product code:SC-0678-25

Gonorrhea Rapid Test – Product code: SC-1187-25 Rapid test for the qualitative detection of gonorrhea antigen on a sample of female cervical and male urethral swabs. For professional in vitro diagnostic use only. The Gonorrhea Rapid Test (Swab) is a rapid immunochromatographic test for the qualitative detection of Neisseria gonorrhea on female cervical and male urethral swab samples to assist in the diagnosis of gonorrhea infection. Gonorrhea is a sexually transmitted disease caused by the Neisseria gonorrhea bacterium. Gonorrhea is one of the most common infectious bacterial diseases and is most frequently transmitted through sexual intercourse, both vaginal, oral and anal. Gonorrhea is a sexually transmitted disease caused by the Neisseria gonorrhea bacterium. Gonorrhea is one of the most common infectious bacterial diseases and is most frequently transmitted through sexual intercourse, both vaginal, oral and anal. Product code:SC-1187-25

Rubella IgM Rapid Test – Product code: IRM-402 A rapid test for the qualitative detection of IgM antibody to Rosolia in human serum or plasma. For professional in vitro diagnostic use only. The Rosolia IgM Rapid Test Cassette is a lateral flow chromatographic immunoassay for the qualitative detection of IgM antibody to Rosolia in whole blood serum or plasma to aid in the diagnosis of Rosolia infection. Rosolia virus is a member of the Togaviridae family, found mainly in human populations. Generally Rosolia is considered a mild adolescence disease. However a maternal infection could be transmitted through the placenta to the fetus, causing congenital Rosolia. Primary Rosolia infection contracted during early pregnancy, may have severe consequences as severe fetal damage, stillbirth or abortion. Children born asymptomatic may develop these abnormalities later in life.1,2 Widespread vaccination has significantly reduced the incidence of Rosolia in all age groups. Product code:IRM-402

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

Hcv Rapid Test – Product code: IHC-402 The Hepatitis C HCV rapid cassette test (whole blood/serum/plasma) is a rapid immunochromatographic test for the qualitative detection of the antibody to the hepatitis C virus in whole blood, serum or plasma. The HCV Cassette Rapid Test Cassette (Whole Blood/Serum/Plasma) is a qualitative membrane-based immunoassay for the detection of antibodies to HCV in whole blood, serum or plasma. The Hepatitis C Virus (HCV) is a single-stranded, small positive sense, encapsulated RNA virus. HCV is now known as the leading cause of parenteral transmission of non-A and non-B hepatitis. The HCV antibody is found in over 80% of patients with widely documented non-A and non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it via an electron microscope. Product code:IHC-402

Adenovirus Rapid Test – Product code: SC-0456-25 The rapid test for Adenovirus (Feces) is a rapid immunochromatographic test for the qualitative detection of Adenovirus in human stool samples to assist in the diagnosis of Adenovirus infection. Acute diarrhea disorder in young children is the leading cause of morbidity worldwide and the leading cause of mortality in developing countries. Research has shown that enteric adenoviruses, especially Ad40 and Ad41, are the leading causes of diarrhea in many of these children, second only to rotaviruses. These viral pathogens have been isolated around the world and can cause diarrhea in babies around one year old. Infections are more common in children under the age of two, but have been found in patients of all ages. Acute diarrhea disorder in young children is the leading cause of morbidity worldwide and the leading cause of mortality in developing countries. Product code:SC-0456-25

Legionella Pneumophila Rapid Test – Product code: SC-0630-25 Rapid test for the qualitative detection of Legionella pneumophila antigen in urine samples. For professional in vitro diagnostic use only. The Legionella pneumophila Rapid Test Cassette (Urine) is an immunochromatographic in vitro diagnostic test. It is designed to detect the soluble Legionella pneumophila serogroup 1 antigen in human urine samples. Legionellosis is severe pneumonia caused by bacteria of the genus Legionella assigned to the Legionellaceae family. This family now includes 48 species and over 60 serogroups. About 20 species are implicated in human diseases. The vast majority of Legionella infections are caused by Legionella pneumophila. Legionnaires’ disease is the main clinical manifestation of Legionella infection, although extra pulmonary infections and non-pulmonary diseases such as Pontiac fever do occur. Product code:SC-0630-25

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

Campylobacter Rapid Test – Product code: SC-0463-10 Rapid test for the qualitative detection of Campylobacter in human stool samples. For professional in vitro diagnostic use only. The Campylobacter Rapid Cassette Test (Feces) is based on the use of a membrane technology with colloidal gold. A nitrocellulose membrane is sensitized with a direct anti-Campylobacter antibody. The specificity of the test is guaranteed by a specific antibody for a Campylobacter antigen conjugated with colloidal gold. Campylobacter enteritis is a zoonotic disease, transmitted through food and water, and is one of the most common causes of infectious diarrhea in the United States. While identification of the causative agent does not typically affect treatment outcomes, as most of these infections are self-limited, laboratory diagnosis is essential for epidemiological studies and for monitoring the outbreak through identification. and strain typing. Product code:SC-0463-10

Antigen Combo Rapid Test – Product code: ISIR-535(SC-2399-20) SARS-CoV-2/Influenza A+B/RSV Antigen Combo Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid protein, Influenza A, Influenza B and Respiratory Syncytial Virus(RSV) antigens present in human nasopharynx. For professional in vitro diagnostic use only. The SARS-CoV-2/Influenza A+B/RSV Antigen Combo Rapid Test (Nasopharyngeal Swab) is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid protein, Influenza A, Influenza B and Respiratory Syncytial Virus(RSV) antigens in nasopharyngeal swab specimens from individuals with suspected SARS-CoV-2/Influenza/RSV infection in conjunction with clinical presentation and the results of other laboratory tests. Results are for the detection of SARS-CoV-2 Nucleocapsid protein, Influenza A+B and RSV Antigens. Product code:ISIR-535(SC-2399-20)

Mononucleosis Rapid Test – Product code: SC-0647-25 Rapid test for the diagnosis of Infectious Mononucleosis (MI) to detect heterophile antibodies to Infectious Mononucleosis qualitatively in whole blood, serum or plasma. For professional in vitro diagnostic use only. The SCREEN MONO rapid test (Whole Blood/Serum/Plasma) is an immunochromatographic test for the qualitative detection of heterophile antibodies to Infectious Mononucleosis in whole blood, serum or plasma to aid in the diagnosis of Infectious Mononucleosis. Infectious Mononucleosis (MI) is caused by the Epstein-Barr virus, which is a member of the herpesvirus family. Symptoms of MI are fever, sore throat, and swollen lymph nodes. In very rare cases, heart or central nervous system problems can occur. Diagnosis of MI is made based on the presence of heterophile antibodies. Infectious Mononucleosis heterophile antibodies belong to the IgM class. Product code:SC-0647-25

Tuberculosis Rapid Test – Product code: SC-0739-40 Rapid test for the qualitative detection of anti-TB antibodies (IgG, IgM and IgA isotypes) in whole blood, serum or plasma samples. The Rapid Tuberculosis Test (Whole Blood/Serum/Plasma) is a qualitative, solid phase, direct, two-site immunoassay for the detection of anti-TB antibodies in whole blood, serum or plasma samples. The membrane is pre-coated with recombinant TB antigen on the line in the test region of the media. During the test, anti-TB antibodies, if present in the whole blood, serum or plasma sample, react with the particles coated with recombinant TB antigen. The compound migrates upwards on the membrane chromatographically by capillary action reacting with the recombinant TB antigen on the membrane and generates a colored line. The presence of this colored line in the test area indicates a positive result, while its absence indicates a negative result. Product code:SC-0739-40

Rubella Igm Rapid Test – Product code: IRM-302(SC-0685-40) Rapid test for the qualitative detection of Rubella IgM antibodies in human serum or plasma. For professional in vitro diagnostic use only. The Rubella IgM rapid test is a rapid immunochromatographic test for the qualitative detection of Rubella IgM antibodies in serum or plasma to assist in the diagnosis of Rubella infection. The Rubella virus is a member of the Togaviridae family, found mainly in human populations. Rubella is generally considered to be a non-serious adolescent disease. However, a maternal infection can be transmitted to the fetus through the placenta, causing congenital rubella. A primary rubella infection contracted during the early stages of pregnancy can have serious consequences such as severe damage to the fetus, stillbirth or miscarriage. Babies born asymptomatic can develop these abnormalities later in life. Product code:IRM-302(SC-0685-40)

Ns1 Zika Rapid Test – Product code: SC-0760-40 The NS1 Zika rapid test (Whole Blood/Serum/Plasma) is a rapid immunochromatographic test for the qualitative detection of NS1 antigen of the Zika virus in whole blood, serum or human plasma, an adjunct to the diagnosis of Zika infections. The Zika virus (ZIKV) is a member of the Flaviviridae family of viruses. It is spread through daytime active Aedes mosquitoes, such as A. aegypti and A. albopictus. The name comes from the Zika forest in Uganda, where the virus was first isolated in 1947. The Zika virus (ZIKV) is a member of the Flaviviridae family of viruses. It is spread through daytime active Aedes mosquitoes, such as A. aegypti and A. albopictus. The name comes from the Zika forest in Uganda, where the virus was first isolated in 1947. The Zika virus is linked to dengue, yellow fever, Japanese encephalitis and West Nile viruses. Since the 1950s it has been known to spread in the area of ​​the equatorial strip from Africa to Asia. Product code:SC-0760-40

Ambroplast dispone di moderne presse ad iniezione da 160 a 1500 ton. complete di robot e deumidificatori per il trattamento di tutti i tipi di resine termoplastiche.

Multi Drug Rapid Test Oral Fluid – Product code: SC-0005-25 Anti-drug test that detects 10 substances by saliva: cocaine, opiates, marijuana (THC cannabinoids), K2 synthetic drugs, ketamine, amphetamines, metanphetamines, MDMA ecstasy, methadone and alcohol. Screen CUP 10-S is a drug test with a reliability of 98%. This product is equipped with a built-in test binder that can be read from our printing tool that is offered for free. Possibility of reading the test also visual without instrument. Present in the test the control line (C) for the correct execution of the test. This drug testigates also analyzes alcohol through an alcohol test included in the test. Product code:SC-0005-25

Multi Drug Rapid Test Cup – Product code: SC-0302-25 Cup / Glass version drug test. The drug test analyzes the following substances: Barbiturates, Buprenorphine, Benzodiazepines, Cocaine, MDMA (Ecstasy), Methamphetamines, Methadone, Opiates, Oxycodone, Pencyclidine, Propoxyphene, Thc (Marijuana), also checks the validity of the urine sample via an adulteration test present in the test (PH, SG, OX) and the presence of alcohol. It is sold in boxes of 25 pieces. (A form in triplicate is provided with the test). This Drug Test has a result printing system via its software tool (Objective Printing), or the test result can also be scanned or photocopied. Product code:SC-0302-25