https://www.avient.com/industries/transportation/aerospace/cargo-containers
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/sites/default/files/2022-04/MEVOPUR LQ for Silicone Elastomers.pdf
Values reported as “typical” or stated without a range do not state minimum or maximum properties; consult your sales
representative for property ranges and min/max specifications.
Processing conditions can cause material properties to shift from the values stated in the information.
Avient products have not been designed for nor are they promoted or intended for use in:
(a) medical devices categorized by either the United States Food and Drug Administration (FDA) or the International Standards Organization (ISO) as an “implant” device; or “Permanent” as defined under
US Pharmacopoeia (USP) or ISO standards; or
(b) active implantable medical devices as defined in EU Directive 90/385/EEC as amended; or
(c) medical devices for “Long Term” use as defined in EU Directive 93/42/EEC as amended.
https://www.avient.com/company/sustainability/sustainability-report/products/product-stewardship-global-chemical-management-product-excellence
We continue to actively monitor the developing regulatory activities at state, national and global levels with respect to per and polyfluoroalkyl substances (PFAS).
PFAS covers thousands of different substances and definitions of PFAS differ across organizations, states, and countries.
International standards cover areas of Quality, Environmental, Health and Safety, Automotive, Medical Device, Responsible Care® and Energy Management.
https://www.avient.com/industries/healthcare/remote-monitoring-wearables/continuous-glucose-monitors-cgm
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/sites/default/files/2021-10/remafin-ep-white-masterbatches-for-pharma-application-bulletin_0.pdf
Values reported as “typical” or stated without a range do not state minimum or maximum properties; consult your sales
representative for property ranges and min/max specifications.
Processing conditions can cause material properties to shift from the values stated in the information.
Avient products have not been designed for nor are they promoted or intended for use in:
(a) medical devices categorized by either the United States Food and Drug Administration (FDA) or the International Standards Organization (ISO) as an “implant” device; or “Permanent” as defined under
US Pharmacopoeia (USP) or ISO standards; or
(b) active implantable medical devices as defined in EU Directive 90/385/EEC as amended; or
(c) medical devices for “Long Term” use as defined in EU Directive 93/42/EEC as amended.
https://www.avient.com/news/connected-safer-and-smarter-polyone-collaborates-halo-smart-labs-next-gen-home-safety-devices
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Connected, Safer, and Smarter: PolyOne Collaborates with Halo Smart Labs on Next-Gen Home Safety Devices
CLEVELAND – PolyOne recently worked with Halo Smart Labs in launching Halo and Halo+, devices that go beyond standard smoke alarms by combining home automation with safety technology.
These modern life savers rely on Resilience™ LS, PolyOne’s latest rigid vinyl material formulated for smart home (IoT) devices.
https://www.avient.com/news/polyone’s-new-bio-based-solutions-deliver-performance-and-sustainability-goals
Geon BIO materials are formulated with PolyOne’s plant-based reFlex™ 300 plasticizer, which has been tested and certified by the United States Department of Agriculture’s BioPreferred® Program to be 99 percent bio-based.
In addition, specific Geon BIO healthcare formulations are pre-certified to meet biocompatibility requirements for United States Pharmacopeia (USP) Class VI protocols.
https://www.avient.com/industries/building-construction/power-management
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/news/polyone-features-more-materials-approach-medical-devices-mdm-west-2020
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PolyOne Features a “More Than Materials” Approach for Medical Devices at MD&M West 2020
ANAHEIM, Calif. – February 3, 2020 – At Medical Design and Manufacturing (MD&M) West next week, PolyOne is focusing on helping customers solve pressing medical device challenges through a “More Than Materials” approach.
The portfolio also boasts the addition of Versaflex™ HC BT218, a new biopharmaceutical tubing grade developed in response to supply challenges and sterilization concerns for an array of medical devices
https://www.avient.com/sites/default/files/2022-12/Mevopur Healthcare Bio-based Polymer Solutions Application Bulletin.pdf
Values reported as “typical” or stated without a range do not state minimum or maximum properties; consult your sales
representative for property ranges and min/max specifications.
Processing conditions can cause material properties to shift from the values stated in the information.
It is the responsibility of the medical device manufacturer and the person placing the medical device on the market to ensure compliance of the medical device with all applicable laws and regulations, including
the suitability of all raw materials and components used for its manufacture.