Multi Line Drug Rapid Test Cassette – Product code: SC-0265-25
Anti-drug test that detects 10 substances via urine: Buprenorphine, fenciclidine, antidepressants TCA, Tramadol, Ketamine, EDDP, Fentanil, K2 synthetic drugs, proposxifen, oxycodone. (The 120ml urine container is supplied separately, you can buy it on the “Accessories” page).
Product code:SC-0265-25
Genject brand disposable syringes with seals are produced untouched by hand in accordance with ISO 13485 and CE standards in a new production facility equipped with a 2021 model machine park and state-of-the-art technology in a closed area of 18.000 m².
Genject brand syringes with seal have a shelf life of 5 years with ethylene oxide (EO) gas sterilization method.
It is non-toxic and pyrogen-free with centric or eccentric body options thanks to its 6% inclined Luer tip.
Genject branded syringes always prioritize quality by facilitating the movement of the piston, thanks to the specially designed Medical Grade silicone in the body.
Dimensions:2 ML 27 G / 50 mm 3P Syringe
All patients drapes of this pack are absorbent and impermeable on their entire surface. The contents of the pack are wrapped within a transfer drape. All gowns of this package are full ultrasonic welding.
Weight of the pack:700 g. All sizes are customizable.
Stock code:300-002
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
Multi Drug Rapid Test Oral Fluid – Product code: SC-0852-25
Available in the version of 7 substances that analyzes through saliva: opiates (40 ng/ml), hydrocodone and oxycodone (40 ng/ml), cocaine (30 ng/ml), cannabinoids (THC) (25 ng/ml), amphetamines (40 ng/ml), methamphetamine (40 ng/ml), MDMA ecstasy (50 ng/ml). Quick chromatographic immunological test for the qualitative identification of multiple drugs and their metabolites in saliva, are included in the analyzed substances: morphine (40 ng/ml), codeine (40 ng/ml), Didrocodeine (40 ng/ml), 6-MAM (4 ng/ml), MDA MDEA MBDB (50 ng/ml), benzailecgonine (30 ng/ml), etc. Screen Cube 7-S is a test drug with CE mark, respects the legislative decree 8 September 2000 No. 332 implementation of Directive 98/79 CE, IVD test, notified at the Ministry of Health, with a reliability of 98%.
Product code:SC-0852-25
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
Genject brand disposable syringes with seals are produced untouched by hand in accordance with ISO 13485 and CE standards in a new production facility equipped with a 2021 model machine park and state-of-the-art technology in a closed area of 18.000 m².
Genject brand syringes with seal have a shelf life of 5 years with ethylene oxide (EO) gas sterilization method.
It is non-toxic and pyrogen-free with centric or eccentric body options thanks to its 6% inclined Luer tip.
Genject branded syringes always prioritize quality by facilitating the movement of the piston, thanks to the specially designed Medical Grade silicone in the body.
Dimensions:1 ML 25 G / 16mm 3P Syringe
Multi Drug Rapid Test Oral Fluid – Product code: SC-0388-25
Drug test by saliva, detects the following substances: opiates and metabolites, cocaine and metabolites, marijuana cannabinoids (THC), amphetamine, mdma and methadone. Screen 6-S is a test drug with CE mark, respects the legislative decree 8 September 2000 No. 332 implementation of Directive 98/79 EC, Test IVD, notified at the Ministry of Health, with a reliability of 98%. This product is equipped with a binder with a separate test that can be read from our printing tool that is offered free of charge. Possibility of reading the test also visual without instrument. Present in the test the control line (c) for the correct execution of the test.
Product code:SC-0388-25
Multi Drug Rapid Test Cup – Product code: SC-0203-25 – SC-0814-25
Drug test in Bicchierino which analyzes the substances required by the state-regions agreement of 09/18/08 (law for occupational medicine) through urine and also analyzes Buprenorphine as required by the additional note of the Lombardy region. SCREEN CUP 8 + AD analyzes the required substances with the cut-offs indicated by the law and has incorporated in the test the control of Creatinine and Ph. Analyzes: Cocaine and metabolites (COC 300), Amphetamine (AMP 500), Methamphetamine (MET 500) , Buprenorphine (BUP 10), Marijuana (including cannabinoids THC) (THC 50), opiates (including heroin morphine and metabolites) (MOP 300), Methylenedioxymethamphetamine Ecstasy (MDMA 500), Methadone (MTD 300), also check the validity of the sample urine via an adulteration test present in the test. It is sold in boxes of 25 pieces.
Product code:SC-0203-25 – SC-0814-25
One Step Drug Test Card – Product Code: SC-2047-25
The Screen 1 Tramadol rapid test (TML) (Urine) is a rapid immunochromatographic test for the qualitative detection of Tramadol in human urine at a concentration of 100 ng / mL. It is a clinical exam intended for use by health professionals, including those in outpatient clinics. This test will identify other related compounds, please refer to the Analytical Specificity table in this package insert. Tramadol (TML) is a quasi-narcotic analgesic used in the treatment of moderate to severe pain. It is a synthetic analogue of codeine, but has a low binding affinity for μ-opioid receptors. High doses of Tramadol can induce tolerance and psychological dependence and lead to abuse. Tramadol is extensively metabolized after oral intake. About 30% of the dose is excreted in the urine as an unchanged drug, while 60% of the dose is excreted as metabolites.
Product code:SC-2047-25
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
Genject brand disposable syringes with seals are produced untouched by hand in accordance with ISO 13485 and CE standards in a new production facility equipped with a 2021 model machine park and state-of-the-art technology in a closed area of 18.000 m².
Genject brand syringes with seal have a shelf life of 5 years with ethylene oxide (EO) gas sterilization method.
It is non-toxic and pyrogen-free with centric or eccentric body options thanks to its 6% inclined Luer tip.
Genject branded syringes always prioritize quality by facilitating the movement of the piston, thanks to the specially designed Medical Grade silicone in the body.
Dimensions:2,5 ML 27 G / 50 mm 3P Syringe
Genject brand disposable syringes with seals are produced untouched by hand in accordance with ISO 13485 and CE standards in a new production facility equipped with a 2021 model machine park and state-of-the-art technology in a closed area of 18.000 m².
Genject brand syringes with seal have a shelf life of 5 years with ethylene oxide (EO) gas sterilization method.
It is non-toxic and pyrogen-free with centric or eccentric body options thanks to its 6% inclined Luer tip.
Genject branded syringes always prioritize quality by facilitating the movement of the piston, thanks to the specially designed Medical Grade silicone in the body.
Dimensions:2,5 ML 23 G / 25 mm 3P Syringe
Screen Led Mask face and neck for skin’s natural biorestructuring, treatment based on red light (660nm), blue light (415nm), orange light (590nm) and infrared light (850nm).
Free-sale product not intended for medical purposes.
PHARMACIST CODE:922411689
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
One Step Drug Test Card – Product Code: SC-0036-25
The Benzodiazepine Rapid Screen 1 Test (Urine) is a rapid chromatographic immunoassay for the detection of Oxazepam (main metabolite) in the urine at a threshold-limit concentration of 300ng/ml. This test will detect other related compounds, please refer to the Analytical Specificity table in this package insert. Benzodiazepines are drugs frequently prescribed for the symptomatic treatment of anxiety and sleep disorders. They produce their effects through specific receptors involving a neurochemical called gamma aminobutyric acid (GABA). Due to their increased safety and efficacy, benzodiazepines have replaced barbiturates in the treatment of anxiety and insomnia. Benzodiazepines are also used as sedatives before surgery and medical procedures and for the treatment of seizures and alcohol withdrawal.
Product code:SC-0036-25
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
Genject brand disposable syringes with seals are produced untouched by hand in accordance with ISO 13485 and CE standards in a new production facility equipped with a 2021 model machine park and state-of-the-art technology in a closed area of 18.000 m².
Genject brand syringes with seal have a shelf life of 5 years with ethylene oxide (EO) gas sterilization method.
It is non-toxic and pyrogen-free with centric or eccentric body options thanks to its 6% inclined Luer tip.
Genject branded syringes always prioritize quality by facilitating the movement of the piston, thanks to the specially designed Medical Grade silicone in the body.
Dimensions:2,5 ML 22 G / 38 mm 3P Syringe
One Step Drug Test Card – Product Code: SC-2061-25
The Screen 1 MDPV Rapid Immersion Test (Urine) is a rapid immunochromatographic test for the qualitative detection of 3,4 methylenedioxypyrovalerone in human urine at a concentration of 1000 ng/mL. 3,4-Methylenedioxypyrovalerone (MDPV) is a psychoactive recreational drug with stimulating properties that acts as a norepinephrine-dopamine reuptake inhibitor (NDRI). It was first developed in the 1960s by a team from Boehringer Ingelheim. MDPV remained an unknown stimulant until 2004, when it began to be sold as a designer drug. Products labeled MDPV-containing bath salts were initially sold as recreational drugs at gas and food stations in the United States, as was the case with Spice and K2, which were sold as incense.
Product code:SC-2061-25
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
Rapid test for the qualitative detection of Helicobacter pylori (H.pylori) antigens in human feces. For professional in vitro diagnostic use only. The rapid test for H. pylori antigen (Feces) is a chromatographic immunoassay for the qualitative identification of H. pylori antigens. pylori in stools to aid in the diagnosis of H. pylori infection. The H. pylori is a small coiled bacterium that lives on the surface of the stomach and duodenum. It is involved in the etiology of various gastrointestinal disorders, including duodenal and gastric ulcers, non-ulcer dyspepsia and acute and chronic gastritis. Both invasive and non-invasive methods are used to diagnose H. pylori infection in patients with symptoms of gastrointestinal diseases. Sample and costly invasive diagnostic methods include gastric or duodenal biopsy followed by urease test (presumable), culture and / or histological section.
Product code:SC-0616-25