Finden Sie schnell prüftechnik für Ihr Unternehmen: 129 Ergebnisse

Dichtigkeitsprüfungen für Gehäuse mit Elektroniken mit der 1. Kennziffer: IP 0X bis IP 6X. IP-Schutzartenprüfungen (Schutz gegen Eindringen von Fremdkörpern) Wir prüfen Ihr Baumuster auf Schutz gegen Eindringen von Fremdkörpern. In unseren Laboren decken wir die gesamte Bandbreite der Schutzartenprüfung in den Klassen IP1X bis einschließlich der Prüfung IP6X. Unsere IP-Schutzartenprüfungen umfassen: - IP 0X = Nicht geschützt - IP 1X = Schutz gegen Eindringen von festen Fremdkörpern mit einem Durchmesser > 50 mm - IP 2X = Schutz gegen Eindringen von festen Fremdkörpern mit einem Durchmesser > 12,5 mm - IP 3X = Schutz gegen Eindringen von festen Fremdkörpern mit einem Durchmesser > 2,5 mm - IP 4X = Schutz gegen Eindringen von festen Fremdkörpern mit einem Durchmesser > 1,0 mm - IP 5X = Geschützt gegen Staub in schädigender Menge - IP 6X = Staubdicht Beispielhafte Normen: - DIN 40050-9 (Achtung: Norm zurückgezogen) - DIN EN 60529 - DIN EN 60068-68 - RTCA DO 160E

Grösse M3-M20, Artikelnummer: uni0102 Es werden hoch präzise Linearführungen eingesetzt. Die Anpresskraft ist stufenlos einstellbar. Es werden hoch präzise Linearführungen eingesetzt. Die Anpresskraft ist stufenlos einstellbar.

Video-Mess-System. Dieses Einstiegssystem bietet eine einfache Messung. Sein Platzbedarf und sein geringes Gewicht machen es besonders praktisch für die Werkstatt. Seine einfache Bedienung ist eine Bereicherung für jeden Anwender. N°: MA 331-075-14 Technische Daten: Basis aus Guss Manueller Kreuztisch MA 142-2, Verfahrweg 25 x 25mm. Mechanische Genauigkeit 0.005mm / 25mm. Rundtisch integriert. Digitale Mikrometern BST. Leseauflösung 0.001mm. Säule mit Schnellverstellung. Zoom-Optik 6.5X mit 4 Rasterindexen. Farbkamera 1.3 Mpx USB 3.0. Bildschirm 24". LED Beleuchtungen. Masse (BxTxH): 290x390x580mm. Gewicht: 19kg.

Corona-Virus-Testung ------------------------------- Testen gegen behüllte Viren als Ersatz für die derzeit nicht verfügbare kommerzielle Teststrategie gegen 2019-nCov / SARS-CoV-2 Da das neue SARS-CoV-2 Virus zu den behüllten Viren gehört, bietet die INVITRO-CONNECT GmbH die Durchführung von Testungen diverser Oberflächen und Desinfektionsmittel gegen das Vaccinia Ankara Virus (MVA) als Referenzvirus behüllter Viren an, als auch gegen das bovine Coronavirus an, das ebenso wie das SARS-CoV-2 der Gattung Betacoronavirus angehört. Es werden neben Standardtestungen für Oberflächen gemäß ISO 21702 (glatte Oberflächen) und ISO 18184 (raue Oberflächen) sowie Suspensionsversuche für den Desinfektionsmittelbereich ( EN ISO 14476/16777) auch weitere Prüfungen auf Anfrage angeboten (s.u.) Benannte Tests sind derzeit die state-of-the-art Prüfmethoden für die Testung gegen 2019-nCov / SARS-CoV-2, da es gegen das 2019-nCov / SARS-CoV-2 Virus selbst, derzeit noch kein spezifisches Testverfahren gibt. Darüber hinaus bieten wir an: Wirksamkeitsprüfungen u.a. von Desinfektionsmittel (inkl. mikrobieller Testung) Antiseptika als Instrumenten-, Reinigungs- und Desinfektionsmittel gegen Viren, Bakterien, Bakteriophagen, Hefen, Schimmelpilze und Mycobakterien und Bakteriensporen nach allen deutschen und europäischen Prüfverfahren sowie auch nach z.B. ASTM oder JIS in der humanen Medizin- , Veterinärmedizin, bei Biozidprodukten im Falle von Oberflächen- und Händedesinfektionsmitteln, Lebensmittel und Kosmetika. Neben antimikrobieller auch (anti-) adhäsive und Eigenschaftsprüfungen von Oberflächen. Spezialtests und andere Prüfgegenstände (Wasser, Lebensmittel) gerne auf Anfrage.

Corona virus testing ------------------------------- Testing against enveloped viruses as a replacement for the currently unavailable commercial test strategy against 2019-nCov / SARS-CoV-2 Since the new SARS-CoV-2 virus is one of the enveloped viruses, INVITRO-CONNECT GmbH offers testing of various surfaces and disinfectants against the Vaccinia Ankara Virus (MVA) as a reference virus for enveloped viruses, as well as against the bovine coronavirus , which, like SARS-CoV-2, belongs to the genus Betacoronavirus. In addition to standard tests for surfaces in accordance with ISO 21702 (smooth surfaces) and ISO 18184 (rough surfaces) as well as suspension tests for the disinfectant area (EN ISO 14476/16777), other tests are also offered on request (see below). Named tests are currently the state-of-the-art test methods for testing against 2019-nCov / SARS-CoV-2, as there is currently no specific test procedure against the 2019-nCov / SARS-CoV-2 virus itself. We also offer: Effectiveness tests of disinfectants (including microbial testing) antiseptics as instruments, cleaning agents and disinfectants against viruses, bacteria, bacteriophages, yeasts, molds and mycobacteria and bacterial spores according to all German and European test methods as well as e.g. ASTM or JIS in human medicine -, veterinary medicine, in the case of biocidal products in the case of surface and hand disinfectants, food and cosmetics. In addition to antimicrobial, (anti-) adhesive and property tests of surfaces. Special tests and other test items (water, food) on request.

OECD 435 - Skin Corrosion : "In Vitro Membrane Barrier Test Method for Skin Corrosion" (Corrositex) Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining skin Corrosion: - OECD 435 - Skin Corrosion : "In Vitro Membrane Barrier Test Method for Skin Corrosion" (Corrositex): The Corrositex® assay is a standardized and quantitative in vitro test developed as a replacement for the dermal corrosivity rabbit test. The Corrositex® assay is presently the only in vitro assay approved by the U.S. Department of Transportation for testing potential corrosive materials and assigning packing group categories. For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com More than 80 test laboratories - Product safety - Regulatory service - In vitro tests - All OECD tests for pharmaceuticals, chemicals, medical devices and cosmetics - Study monitoring, MSDS etc. #projectmanagement #study #chemicals #biocides #cosmetics #pharma #regulatory #toxicological #laboratory #reach #medical #invitro #OECD431 #OECD439 #OECD435 #testing #test #labor

Test Guideline No. 439 OECD 439 / in Vitro Skin Irritation Reconstructed Human Epidermis Test Method Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining Skin Irritation: - OECD 439 / Skin Irritation Test (SIT) in a Reconstructed Human Epidermis (RhE) Model - Skin Irritation in the regulatory hazard classification and labeling context is defined as the production of reversible damage to skin following a defined chemical exposure. The Skin Irritation Test (SIT) is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing moderate skin irritation (UN GHS Category 2 Skin Irritants1), and to discriminate UN GHS Category 2 Skin Irritants from UN GHS 3 Mild Skin Irritants as well as those not requiring classification for skin irritation potential. This test method is useful for regulatory classification and labeling of chemicals and mixtures, and depending upon the regulatory jurisdiction and framework the test results may be used as standalone or to support a weight of evidence approach. Since skin irritation in vivo typically results from chemical-induced cell damage and subsequent inflammatory cascade, this test method provides a mechanistically-relevant measurement of cell viability in reconstructed human epidermis (RhE) tissues after a single topically-applied chemical treatment, relative to negative control-treated tissues. Chemicals which reduce relative viability to ≤ 50% would be classified as an irritant (and a potential corrosive), while those which result in a relative viability > 50% would not be classified as a skin irritant in accordance with UN GHS Category 2. INVITRO-CONNECT GmbH has extensive expertise with a wide variety of reconstructed skin-based protocols. NOTE: Since this test method does not discriminate UN GHS categories 1 and 2, an irritant prediction by this test method should be followed up with a test for potential skin corrosion, using any of the validated corrosivity test methods. 1) Corrositex Membrane Barrier Time Monitor Corrosion Test Method and 2) In Vitro Skin Corrosion Test using a Reconstructed Human Epidermis (RhE) Model A variety of other protocols are available to evaluate for potential skin irritation to support product development, product stewardship, candidate formulation selection and other non-regulatory applications, and can provide a rank ordering of skin irritation potential. A variety of protocols allow for evaluation of mild formulations: 1) Time-to-Toxicity ET50 Screening protocol, and 2) Cytokine Expression Assay for Mild Products and for moderate to corrosive products and mixtures: 3) In Vitro Skin Irritation / Corrosion Screen. For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com More than 80 test laboratories - Product safety - Regulatory service - In vitro tests - All OECD tests for pharmaceuticals, chemicals, medical devices and cosmetics - Study monitoring, MSDS etc.

Microbiological tests against viruses, bacteriophages, bacteria, yeast, molds, mycobacteria and bacterial spores for disinfectants, medical devices, pharmaceutical products and cosmetics Microbiological examinations: ------------------------------------------------ Microbiological tests against viruses, bacteriophages, bacteria, yeast, molds, mycobacteria and bacterial spores. Our team of experts supports manufacturers of biocidal and medical products as well as cosmetics and pharmaceuticals scientifically in the context of approval projects. For example, we create safety assessments for cosmetics and biocompatibility assessments for medical devices. Here we focus in particular on infection prevention and wound treatment products.

OECD 431 Test Guideline No. 431 In Vitro Skin Corrosion: Reconstructed Human Epidermis (RhE)Test Method Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com INVITRO-CONNECT GmbH offers various test strategies without animal testing for examining skin Corrosion: - OECD 431 - Human Skin Corrosion: "In Vitro OECD 431: Reconstructed Human Epidermis Test Method, in vitro Test - Skin Corrosion in the regulatory hazard classification and labeling context is defined as the production of irreversible damage to skin, generally evident as necrosis through the epidermis and into the dermis, following a defined chemical exposure. The In Vitro Skin Corrosion Test is an in vitro, non-animal test designed to identify those chemicals and mixtures capable of inducing skin corrosion (UN GHS Category 11), and in some cases to partially subcategorize corrosives into UN GHS Sub-Categories 1A or 1B and 1C (ie., the current test methods do not effectively discriminate between UN GHS Sub-Categories 1B and 1C). This test method is useful for regulatory classification and labeling of chemicals and mixtures, and depending upon the regulatory jurisdiction and framework the test results may be used as standalone or to support a weight of evidence approach. Since skin corrosion in vivo typically results from rapid chemical-induced cell damage, this test method provides a mechanistically-relevant measurement of cell viability in reconstructed human epidermis (RhE) tissues after a single topically-applied chemical treatment, relative to negative control-treated tissues. INVITRO-CONNECT has extensive expertise with a wide variety of reconstructed skin-based protocols. NOTE: Since this test method does not discriminate among any non-corrosive categories, a non-corrosive prediction by this test method should be followed up with a test for potential skin irritation, using any of the validated Skin Irritation Test (SIT) methods, including the In Vitro Skin Irritation Test using a Reconstructed Human Epidermis (RhE) Model. For more information please contact INVITRO-CONNECT GmbH for assistance in developing specialized protocols for your test materials. INVITRO-CONNECT GmbH: Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com More than 80 test laboratories - Product safety - Regulatory service - In vitro tests - All OECD tests for pharmaceuticals, chemicals, medical devices and cosmetics - Study monitoring, MSDS etc.