Produse pentru testează (264)

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

La Crema Anti-Age viso e Contorno occhi Staminax è un'innovativa soluzione per chi cerca un trattamento efficace contro i segni del tempo. Questa crema combina ingredienti tradizionali della cosmetica con attivi all'avanguardia, offrendo una performance anti-age rivoluzionaria. Grazie a un preparato brevettato di due principi attivi estratti da cellule staminali vegetali, la crema offre una tripla azione che migliora l'elasticità della pelle, riduce le rughe e attenua le occhiaie. Sviluppata e prodotta in Italia da esperti del settore farmaceutico e cosmetico, questa crema è il risultato di anni di ricerca e innovazione. La formula della Crema Anti-Age viso e Contorno occhi Staminax è arricchita con Olio d'Argan, Olio di Jojoba, Olio di Vinaccioli e Burro di Karité, tutti ingredienti naturali e biologici che nutrono e idratano la pelle in profondità. Con il 99,8% di ingredienti naturali e il 50,2% di ingredienti biologici, questa crema è priva di profumi, parabeni, OGM e derivati animali, rendendola adatta anche per le pelli più sensibili. Dermatologicamente testata e clinicamente provata, la crema è vegana e non testata su animali, garantendo un trattamento sicuro ed efficace per una pelle visibilmente più giovane e luminosa.

This unit was designed and built for protection of workstations mobile or permanent on the battlefield or in defense of sen- sitive targets, air-transportable as it is of limited weight and size. Aimed at the protection of operators armed. Front tilted 30 degrees with 8 mm x 70 mm slots suitable for hooking the side panels. Side panels dimensions 1000 x 1000 mm base 900 mm hypotenuse 970mm. Certification: Banco Nazionale di Prova per le Armi da Fuoco Portatili e per le Missioni Commerciali: - Prot. N°22/BAL-AG/vp February 23, 2010. Bullet ballistic resistors 5.56 x 45 SS109 + 7.62x51 Nato. Weight :88,00 kg Hooks:SNAP A BAYONET Color painting: NATO green RAL 6020, - RAL 1002, - other colors on request

Micro-Sampling-Entwicklungsservice zum Testen des Marktes. Diese Art von Service ermöglicht eine originalgetreue Nachbildung des Produkts im industriellen Maßstab, jedoch mit minimalem Inhalt.

GWALKIN Modular Environmental Test Chambers, Galli Original Design - GALLI's GWALKIN model presents optimal testing conditions, These Walk-In Climatic Test Chambers boast a variety of features and advantages tailored to meet the diverse needs of product testing. Available in volumes from 5m3 to 40m3, equipped with precise temperature & humidity control, and lighting management, they serve as an exceptional choice for stability testing across industries such as Pharma, Food & Beverage, Cosmetics, and Material Testing. Moreover, they are suitable for conducting extreme tests in Automotive, Aeronautical, and various other industrial tests. GWALKIN ensure the ideal testing environments across a broad spectrum of temperatures, from sub-zero levels to high temperatures, with precise control over relative humidity, from minimal values to saturation points. In the pharmaceutical sector, our Walk-In Chambers cater to both long-term and accelerated stability testing conditions, according to ICH Q1A (R2) standard for new drug substances and drug products.

A touch of innovation The new T8990 leak tester was designed to improve what was considered the best device in ForTest's history, the M8990. The new video controller “ForTest MMI” brought a superior level of human-machine interaction, thanks to an innovative capacitive panel in tempered glass, around a splendid 6.2” colour display. Parameter programming is much faster thanks to the new numerical keyboard integrated in the menus, and the big display makes viewing even clearer of the test cycle. The main screen also enables interaction with shortcut functions, such as test program change, "smart" test archive menu and locking/unlocking using a password. Limitless connectivity. The new T8990 equipment includes ports for the USB slave, RS232, RS485, Can bus, TTY, Profinet and EtherCAT. Assembly may also include an optional Ethernet port and a 26-pole connector with 4 inputs and 8 outputs, which are completely programmable, for interfacing with the external valves, safety barriers

Quadrettatori per controlli di adesione su rivestimenti singoli e multistrato. Questi strumenti operano la verifica mediante una procedura di creazione manuale di un reticolato quadrato sullo strato di vernice o riporto. Esso si crea facendo scorrere due volte la testina sulla superficie campione. Gli scorrimenti devono essere ortogonali l’uno all’altro, creando così un reticolato quadrato di varie dimensioni, a seconda delle caratteristiche della testina utilizzata per la prova. Dopo aver reato il reticolato si effettua l'ispezione della superfice (con l’aiuto del pennello e lente di ingrandimento), e si compara il risultato con i riferimenti normativi definendo così il grado di adesione.

Tutta la gamma dei nostri diluitori può comunicare con un PC remoto (master) ed acquisire i segnali di misura degli analizzatori in corso di verifica. E' quindi disponibile un pacchetto software che consente l'esecuzione automatica, secondo programma, delle prove di linearità. Lo stesso pacchetto è compatibile con tutta la gamma dei diluitori BetaCAP e con le relative opzioni (MTGS Modulo di selezione per bombole multiple). Il risultato finale della prova, non necessariamente presenziata dall'operatore, è un verbale su formato editabile che include : specifica degli elementi utilizzati (bombole e analizzatori), listato e trend grafico della prova, risultati in accordo alla Norma EN14181

Temperature from -25°C up to +70°C Configuration Volumes from 25 up to 2300 liters stillFACE Stability test performing controller revoFACE Dynamic performing programmer Shelves Included and variable in quantity according to the model Ventilation Forced ventilation fan Alarms High/Low temperature and humidity Electric Power 220-240V ~ /50 Hz different power available 100% Customizable solution

I sistemi di controllo Sport Devices, nascono da una esperienza ventennale in applicazioni sala prova motori. Offriamo un prodotto evoluto, aggiornato e flessibile; in grado di adattarsi a professionalità, competenza ed esi- genze dei nostri clienti. Ripetibilità nelle prove, customizzazione hw e sw, compatibilità di sonde ed attuatori, totale espandibilità del sistema. I principi su cui, da sempre, amiamo sviluppare i nostri sistemi dedicati al testing motori. • Interfaccia OBD veicolo, Sonde Lambda e controller • Acquisizione espandibile sino a 112 canali • Azionamenti servocomandati • Interfacce di collegamento • Ingressi termocoppie • Prese comandate • Pinze induttive • Telecomando

In funzione dei diversi standard nazionali, siamo in grado di effettuare cicli omologativi, calibrazione controllo motore e testing su direttiva cliente

Queste strip test 16 in 1 rappresentano la soluzione migliore per misurare la qualità della vostra acqua. Possono essere impiegati per una vasta gamma di utilizzi quali acqua potabile, acquari, laghetti privati, acque industriali piscine e spa. Ogni strip presenta sedici quadrati colorati che cambieranno la loro colorazione una volta immersi nell'acqua. Ogni quadrato ha un suo proprio range di valori e varierà il proprio colore autonomamente. Dopo l'immersione della strip, quest'ultima andrà confrontata con le scale di colore presenti sul contenitore del prodotto al fine di determinare i valori della soluzione testata. Questo metodo è perfetto per una lettura facile e veloce dei valori dell'acqua. * Forniamo solo ed esclusivamente le aziende del settore quali distributori, rivenditori, assemblatori e costruttori.

Una parte fondamentale del nostro lavoro è rappresentata dalla prestazione dei nostri servizi direttamente presso il cliente: manodopera specializzata per il montaggio meccanico, assistenza su macchine automatiche e affiancamento nel collaudo presso l'utilizzatore.

The basic equipment consists of an ultrasound generator, which is placed in the hold, and a receiver unit fitted with a microphone to receive the emitted ultrasound signals. It is a non-destructive method, non -invasive, can be used in all weather conditions, and can be used with cargo inside the hold.

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