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/healthcare/drug-delivery-systems/pump-technologies
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/industries/healthcare/medical-devices-equipment/imaging-technology
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/industries/consumer/consumer-discretionary/wearable-technology
Wearable Devices
Mobile Devices
IVD Devices
https://www.avient.com/industries/healthcare/medical-devices-equipment
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/sites/default/files/2024-09/Chemical Resistance Technical Bulletin %281%29.pdf
Whether you are designing for a medical device housing or a surgical device in the operating room, we offer
solutions to meet a wide variety of performance specifications and application needs.
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.
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.
https://www.avient.com/sites/default/files/2023-03/Mevopur Healthcare Functional Additives Nucleating 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.
https://www.avient.com/industries/transportation/aerospace/cargo-containers
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/products/engineered-polymer-formulations/chemical-corrosion-resistant-formulations/trilliant-hc-healthcare-thermoplastics
Prevents Device Cracking
Medical Device Housings
Medical Device Housing