Produse pentru testează (242)

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

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.

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:27,00 kg Hooks:SNAP A BAYONET Material :POLYETHYLENE HD

Micro sampling development service to test the market. This type of service allows the product to be faithfully replicated on an industrial scale, but with minimal content.

La macchina per prove di durezza e scalfiture a carico costante SAAST520/1 permette di effettuare il test di resistenza al graffio, uno degli indicatori più importanti per valutare la durezza dei rivestimenti. La prova comporta una graffiatura controllata, effettuata attraverso una punta su un’area selezionata. Un campione viene fissato e spostato lentamente sotto la punta in modo da graffiare la superficie del rivestimento. In base alle procedure del test, possono essere applicati carichi costanti o variabili per ottenere diversi gradi di rottura, da una semplice traccia alla distruzione dello strato. Questa procedura è uno dei metodi comunemente utilizzati per ottenere i carichi limite relativi alle proprietà adesive dei rivestimenti.

Costruito con due moduli a 30 capillari ciascuno, diluisce tra loro tre gas o miscele (es.: gas da misurare, gas interferente, gas diluente), prestandosi ottimamente sia a prove di linearità che a prove di interferenza. E'costruito in modo simile ai due diluitori che l'hanno preceduto, ma la particolare conformazione (due moduli uguali) ha consentito la realizzazione di una speciale procedura di auto-calibrazione "auto-referenziale" : il termine ed il concetto potrà fare inorridire alcuni metrologi, ma l'operazione è molto interessante, oltre che assolutamente originale. Invito chi possa essere incuriosito a contattarci : avrà tutte le informazioni necessarie a valutare la qualità della nostra innovazione. Essendo l'ultimo nato della serie BetaCAP, questo diluitore è costruito con elettronica più avanzata : la risoluzione delle misure passa da 12 a 16 bit e l'interfaccia utilizza display grafico a colori con touch screen.

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.

Temperature from -25°C up to +70°C Humidity from 10% up to 98% Configuration Volumes from 25 liters up to 2300 liters stillFACE Stability test performing controller revoFACE Dynamic performing programmer Ventilation Forced ventilation fan Rack 1* Height-adjustable Alarms High/Low temperature and humidity Electric Power 220-240V ~ /50 Hz different power available 100% customizable solution

The T9731 is specifically designed for measure the adequate air flow rate in complete adherence to the standard EN 14683 for surgical masks testing. As shown in diagram C.1 on page 12 of the standard EN14683 , the instrument is equipped with two air flow meters of type Mass-flow with scales 0.0...20.0 nLitres/minute (2.12 of diagram - point C.2.1) servo driven valve controlled from the software (10 of the diagram - point C.2.4), and a double gauge / differential pressure measurement (M1 and M2) as expressly indicated in point C.2.2 . In order to comply with both the ISO accreditation standards and the expectations of the reference standard, the pressure measurements in “Differential" mode (or pressure drop) occurs in Pa or Pa/cm2 in case the sample area is set in the menu TST with area different from 1.00 cm2. The connecting "short form" attached to the manuals providesconnection to an external vacuum pump (C.2.3), not provided.

GRUPPI VENTILANTI RAFFREDDAMENTO MOTORE Possiamo proporre soluzioni su misura, adeguandole agli spazi disponibili, oppure fornire accessori standard. Tra queste, in particolare, offriamo solu- zioni standard per sistemi di raffreddamento motore; ventole centrifughe su ruote, con freno, disponibili con diverse portare e potenze: • 4 kW • 5,5 kW • 7 kW • 11 kW I gruppi ventilanti, posso essere inoltre dotati di inverter di controllo, per ren- dere la velocità aria proporzionale a quella del veicolo sul banco prova; otti- mizzando così la simulazione delle condizioni in strada (consigliato per flussi aria >110 km/H) SISTEMI DI ESTRAZIONE FUMI Abbiamo sviluppato sistemi di estrazione fumi adeguati all’utilizzo con il ban- co prova potenza. DIametri maggiorati e maggiore potenza, per una sistema professionale affidabile e durevole: • Motore da 5,5kW • Condotte diametro 250 mm, fino a 1.

Rimor realizza macchine di simulazione vento di marcia per banchi a rulli, in grado di raggiungere alte velocità, di lavorare in condizioni di temperatura con grandi escursioni termiche e di garantire omogeneità di flusso, proprio come richiesto dalle varie normative incluso il WLTP. Les machines vent de marche sont utilisées dans les différents essais avec banc à rouleaux et sont en mesure de générer des flux d’air à haute vitesse dans le plein respect des uniformités et des homogénéités requises par les normes en vigueur y compris le WLTP. Les machines produites par Rimor sont aptes à travailler dans des chambres climatiques et, par conséquent, à des températures bien audessous de zéro, assujetties à des changements constants et rapides de vitesses, accélérations, décélérations et de conditions climatiques. En outre, sur demande, nos machines peuvent être équipées d’un système de régulation de hauteur.

Antibacterial peel-off mat, treated with active ingredient which maintains its protection permanently. It allows to decontaminate accesses and passages to clean and sterile rooms, critical areas, grey areas, modified atmosphere packaging chambers. The antibacterial sticky mats have no limits of application and do not block the normal transit of operators and carts. The antibacterial mat is composed by 30 layers, does not require installation. Thanks to its fully adhesive base, it adheres perfectly to the floor, without the aid of frames. Thanks to its water-based adhesive layer, the carpet can be placed anywhere without leaving residues. Decontamination Mat

FILTRO a 30 MANICHE "CS HF30" - MACCHINE Maniche (numero):d-120x1850 n° 30 Superficie filtrante m²:20 Portata m3/h:3000

Spettrofotometro Automatico per Controllo della Trasmittanza e del Colore, Easy_Spectro_RX è IDEALE per il controllo di qualità di Lenti Plano e RX, Occhiali da Sole, Occhiali Sportivi e da Nuoto, Occhiali da Sci, Visiere per Caschi, Vetro Colorato, Film Plastico e altri Materiali Traslucidi, in qualsiasi ambiente industriale e di laboratorio. L’innovativa interfaccia software di Smart_Premium_Suite combinata con Easy_Spectro_RX agevola l’usabilità da parte dell’operatore e garantisce misurazioni ad elevata velocità (solo 1 secondo). Per maggiori informazioni visita il sito web del prodotto e contatta SmartVision!

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.

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