Mobile Devices Inhalation Devices IVD Devices

Customers have reported that devices made with Versaflex HC TPEs successfully withstood 10,000 antiseptic wipes. Both grades, designed for two-shot injection molding, provide a soft touch and grippy feel to enhance ergonomics, comfort and ease of use for housings of hand-held scanners, patient monitors, infusion pumps, defibrillators, reusable surgical devices and other durable medical devices. NOTE TO EDITORS: Based on a multi-state HAI prevalence survey, the Centers for Disease Control and Prevention (CDC) reports that an estimated 722,000 HAIs per year occur in U.S acute care hospitals (source: http://www.cdc.gov/HAI/surveillance/).

PRNewswire/ -- 5G technology will provide the backbone for a step-change in performance of mobile devices, allowing ultrafast download speeds and the ability to connect billions of devices through a network.  In addition, local and state governments continue to allocate budgets and resources for broadband expansion, and the pending United States

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Mobile Devices Inhalation Devices IVD Devices

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Whether it’s high-use consumer goods or healthcare devices, you need to find materials that can resist degrading when they come into contact with common cleaners and disinfectants.   Chemically Resistant Polymers for Next-Generation Device

Companies placing medical devices and packaged pharmaceuticals on the market need their products to comply with healthcare standards, no matter where their products are sold and no matter where they procure their raw materials. For the plastics used in these medical applications, this can mean compliance with the relevant chapters of the International Organization for Standardization (ISO), the United States Pharmacopeia Class VI (USP VI) the European Pharmacopeia (EP 3.1), and the International Conference on Harmonization (ICH Q3D) standards and guidelines. The raw materials are pre-tested to the relevant chapters of ISO 10991, USP 661, USP Class VI, EP 3.1 and to the ICH Q3D guidelines to help manufacturers increase the certainty of regulatory compliance for their devices and packaging.

Mevopur™ Healthcare Colorants, Functional Additives, and Bio-based Formulations: Manufactured across a global network of ISO 13485 facilities, this broad portfolio is pre-tested to United States Pharmacopeia (USP) Class VI, ISO 10993, USP 661, European Pharmacopeia 3.1, and International Conference on Harmonization (ICH) Q3D protocols. Likewise, Mevopur functional additives can help to protect or enhance the performance of polymers used in medical devices, diagnostics, or pharmaceutical packaging. Pre-tested for USP Class VI compliance, they are excellent for use in specialty medical devices, surgical devices, and other vital healthcare applications.