https://www.avient.com/industries/healthcare/medical-devices-equipment/rehabilitation-equipment
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/industries/healthcare/medical-devices-equipment/surgical-medical-instruments
Mobile Devices
Inhalation Devices
IVD Devices
https://www.avient.com/sites/default/files/2024-09/Terms and Conditions of Sale for Germany.pdf
If Buyer has an alleged claim with respect to a particular portion of the Products stated in Seller’s 3.2 Die Gewährleistungsansprüche verjähren in 12 Monaten ab Gefahrübergang.
Buyer will sign a reasonable confidentiality agreement upon request and ensure its employees are bound by at least equally restrictive confidentiality obligations as those stated herein.
If Buyer has an alleged claim with respect to a particular portion of the Products stated in Seller’s order confirmation, such alleged claim does not entitle Buyer to reject the entire delivery of the Products.
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/sites/default/files/2023-03/Avient Annual Report 2022.pdf
This effort can result in process or operational modifications, the installation of pollution control devices or cleaning up grounds or facilities.
Further, the state and local tax benefit was $2.6 million, 4.0%, driven by a U.S. tax loss.
The fixed income common collective funds consist primarily of publicly traded United States fixed interest obligations (principally investment grade bonds and government securities). 54 AVIENT CORPORATION Level 1 assets are valued based on quoted market prices.
https://www.avient.com/products/polymer-colorants/liquid-color-concentrates/mevopur-lq-liquid-color-additives-healthcare
The Mevopur™ LQ range of liquid color and additive concentrates are specially designed for liquid silicone rubber (LSR) used in medical devices and pharmaceutical packaging.
Liquid color & additive concentrates designed for use in medical devices and pharmaceutical packaging
Liquid color & additive concentrates designed for use in medical devices and pharmaceutical packaging (Chinese language version)
https://www.avient.com/sites/default/files/2023-01/Mevopur Healthcare Colorants and Formulations Special Effects 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.
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/knowledge-base/article/regulatory-issues-0
Manufacturing medical devices?
We support your Device Master File submission for healthcare materials by developing and maintaining U.S.
https://www.avient.com/sites/default/files/2021-06/chemical-resistance-technical-bulletin.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.