is a medical device manufacturer whose pain therapy products help patients manage pain and reduce the use of medications such as opiates.

is a medical device manufacturer whose pain therapy products help patients manage pain and reduce the use of medications such as opiates.

Disinfectant Resistance for Medical Device Housings - Case Study Manufacturer boosts disinfectant resistance for medical device housings using Trilliant HC High Performance Formulations

Special formulations for medical applications. Medical Mannikins

A leading North American medical contact manufacturer faced a challenge when molding the gasket for a contact lens container.  Armed with a new specialty TPE solution, the medical manufacturer handled gasket adhesion with a material that outperformed that not only silicone, but also conventional TPEs.

A leading North American medical contact manufacturer faced a challenge when molding the gasket for a contact lens container.  Armed with a new specialty TPE solution, the medical manufacturer handled gasket adhesion with a material that outperformed that not only silicone, but also conventional TPEs.

A leading North American medical contact manufacturer faced a challenge when molding the gasket for a contact lens container.  Armed with a new specialty TPE solution, the medical manufacturer handled gasket adhesion with a material that outperformed that not only silicone, but also conventional TPEs.

Requirements: Excellent clarity, scratch resistance and exceptional toughness for visualization of medicant levels Avient Distribution HC Portfolio: Acrylic, copolyester, PC 2. Requirements: Thermal conductivity for warming of medicants Trilliant™ Therma-Tech™ Thermally Conductive Formulations Heating system 13 Heat Exchanger 14 Technology Enabled Design Connected medical devices are transforming the way care is delivered by making it simpler, easier, more collaborative, and more data driven. Smart health devices improve patient medication adherence and monitoring

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. Without limiting the generality of this statement, Avient products shall not be used in any medical device application intended for: (1) exposure to human tissue or body fluids for 30 days or greater; (2) “plastic” (cosmetic or reconstructive) surgery use; (3) reproductive implants or any birth control device; or (4) any critical component in a permanently (greater than 30 days) implanted medical device that supports or sustains human life. 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, including the suitability of all raw materials and components used for its manufacture, and with all applicable laws and regulations. 1.844.4AVIENT www.avient.com

These antistatic concentrates can be used to increase the visual appeal of a medical device by avoiding charge-related dust accumulation. APPLICATIONS • Medical devices • Drug delivery devices • Labware KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number level, reducing risk of change REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 and USP biological evaluation - European Pharmacopeia 3.1.3/3.1.5 (polyolefin) - USP (polyethylene) - ICH Q3D elemental impurities • Registered Drug Master File (Type III) and/or Device Master File • Food contact established with FDA/EU* * FDA/EU compliance information available upon request Copyright © 2023, Avient Corporation. 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.