Produse pentru testează (212)

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

Tutti i nostri prodotti sono realizzati presso la nostra sede. Durante il ciclo produttivo dei nostri prodotti sono eseguiti collaudi intermedi. Alla fine del ciclo produttivo sono, invece, eseguiti collaudi a tappeto: il 100% dei nostri prodotti viene sottoposto a collaudo prima della consegna al cliente finale. Su ciascun prodotto sono eseguiti i test che possano verificarne la conformità rispetto alle specifiche del cliente, ai parametri progettuali ed alle norme CEI di riferimento. Tutti gli strumenti utilizzati per il collaudo sono soggetti a taratura presso laboratori certificati Accredia.A titolo puramente esemplificativo ed a seconda della tipologia di prodotto possono essere eseguiti i seguenti test (ed altri non elencati): Test di rigidità dielettrica;

Crema Anti-Age Scopri il Prodotto L'azione anti-age della crema viso e contorno occhi Staminax è determinata dalla sapiente miscelazione di ingredienti della tradizione cosmetica con attivi innovativi. Contiene un preparato brevettato di due principi attivi estratti da cellule staminali vegetali, per una tripla azione, dalla rivoluzionaria performance anti-age. La crema viso e contorno occhi anti-Age Staminax è sviluppata, prodotta e confezionata in Italia da professionisti farmaceutici e cosmetici con esperienza decennale. La Formula I due attivi, sono inclusi in una formula preziosa, con Olio d'Argan, Olio di Jojoba, Olio di Vinaccioli e Burro di Karatè. Per un prodotto sublime 99,8% di ingredienti Naturali 50,2% di ingredienti Biologici Senza Profumo Senza Parabeni Senza OGM Senza derivati animali Vegano Non testato su animali L'Efficacia Il potere Anti-Age della crema viso e contorno occhi Staminax è garantito dall'alto contenuto di estratti da cellule staminali vegetali. Il primo stimola le nostre cellule a produrre collagene normalmente presente nella pelle umana, donando elasticità alla pelle, prevenendo e riducendo le rughe. Il secondo stimola la degradazione della bilirubina riducendo le occhiaie e migliora la microcircolazione riducendo le occhiaie. Gli Studi Sicurezza e Efficacia: Dermatologicamente testato su pelli sensibili, studio condotto su 25 volontari e sotto supervisione di un medico dermatologo. Nichel Tested Testato per altri 8 metalli pesanti Efficacia testa in Vivo, studio condotto su 30 volontari e sotto supervisione di un medico dermatologo. Per aproffondimenti visita il sito :https://www.staminax.it/staminax-antiage.

Le teste per dosatori di polifosfati personalizzate in ottone sono progettate per prevenire calcare e corrosione nelle tubature, offrendo soluzioni affidabili e durature per il trattamento delle acque. Realizzate con ottone di alta qualità, queste teste offrono una resistenza eccezionale alla corrosione e una lunga durata, rendendole ideali per applicazioni domestiche e industriali. La possibilità di personalizzare queste teste secondo le specifiche del cliente garantisce un adattamento perfetto e un funzionamento ottimale, migliorando l'efficienza e la sicurezza dei sistemi in cui vengono utilizzate. Le principali categorie di dosatori di polifosfati includono dosatori a cartuccia, proporzionali, manuali, automatici e per caldaie. Questa varietà di opzioni consente di scegliere la testa più adatta per ogni applicazione specifica, garantendo una protezione efficace contro il calcare e la corrosione. Grazie alla loro robustezza e versatilità, le teste per dosatori di polifosfati personalizzate in ottone rappresentano una soluzione affidabile per qualsiasi progetto che richieda componenti di alta qualità e prestazioni durature nel trattamento delle acque.

Nel reparto produttivo disponiamo un area dedicata alle cernite visive al montaggio manuale e/o in automatico di componenti e prodotti a Disegno tecnico in conto lavoro per il Cliente finale.

Ballistic plate for individual protection. The plate meets ballistic performance only together with the level III ballistic panel. N.I. JSTD0101.04. - Ballistic protection Polyethylene UD; - Caliber bullet: 7.62 Ordinary Born FMJ 9.55, Grams / 856 meters / sec; - Energy 3,476 J; - Impact angle: 90 °; - Test temperature 20 °; - Humidity 70%; ULTRA-HIGH-MOLECULAR-WEIGHT POLYETHYLENE. Weight:1,350 kg Shape:MULTICURVATURE SINGLE CURVATURE BALLISTIC PLATE MATERIAL :100% UHMWPE

Servizio di sviluppo di una micro campionatura per testare il mercato. Questo tipo di servizio permette di replicare in modo fedele il prodotto in scala industriale, ma con minimi contenuti.

Assorbono forze radiali di trazione e compressione, indicati per movimenti lenti con medio piccoli angoli di oscillazione.

The Imeta A1 model is a simple model seamer but nonetheless is equipped with all the necessary features for manufacturing small batches and/or seaming tests. The machine has CE protections as standard, and may be supplied with a CO2 flow device to seam carbonated soft drinks cans. The Imeta A1 seams cans up to a diameter of 190mm and a height of 250mm.

Le perline ad incastro sono delle isolaspine in steatite utilizzate per ricoprire i fili e i terminali di resistenze elettriche che grazie alla loro forma bombata si incastrano l'una con l'altra e permettono di ricoprire cavi e fili con facilità mantenendo la flessibilità del cavo. Materiale:Steatite C221 Temperatura:fino 1200°C

We have a wide range of natural and natural-identical flavours tested by experts enabling us to solve any problem requing these flavourings: Yoghurt Desserts Fruit preparations Flavoured milk beverages Margarine A close cooperation between application technologists and marketing experts enable us to achieve the best possible results for our customers.

Test chamber - Control and testing instrumentation

POSSIBILITA’ DI NOLEGGIO OPERATIVO FINALIZZATO ALL’ACQUISTO (“RENT TO BUY”): non crea una complicata gestione di cespiti patrimoniali e non impatta né sul ricalcolo IRAP né sugli studi di settore si hanno costi certi per tutta la durata contrattuale con possibile opzione di acquisto a prezzo prestabilito ora per allora non si hanno “esposizioni bancarie” in quanto il rapporto è di tipo commerciale privato tra fornitore e cliente Diametro tamburo:520 mm Larghezza tamburo:650 mm Peso massimo di carico:130 kg Volume massimo:52 dm³ Tipo turbina:CM 334 Motore turbina:4kW Tipologia separatore:Pneumautico Potenza elettrica installata:8kW

Valvola a sfera in acciaio ASTM A105, saldare di testa, secondo norme UNI 9734 e EN 13774, per intercettazione di gas naturale, con quadro di manovra.

La nostra azienda è specializzata nello sviluppo di prototipi conto terzi, con l'obiettivo di ampliare il proprio mercato e portare innovazione nel settore delle macchine agricole. Grazie alla nostra esperienza e competenza, siamo in grado di realizzare prototipi personalizzati che rispondono alle specifiche esigenze dei nostri clienti. Collaboriamo strettamente con i nostri partner per garantire che ogni prototipo sia progettato e costruito secondo i più alti standard di qualità e sicurezza.

Corpo per testa di fresatura 450 x 450 x 600 ricavato da fusione in ghisa sferoidale e completamente lavorato su tornio SAFOP e fresatrica SACHMAN

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