In Handbook of Polymer Applications in Medicine and Medical Devices,¹ Laurence W. LSR has a long-standing track record of use in the medical industry. Medical-grade TPEs can rival LSR in biocompatibility performance, depending on their chemistry.

In Handbook of Polymer Applications in Medicine and Medical Devices,¹ Laurence W. LSR has a long-standing track record of use in the medical industry. Medical-grade TPEs can rival LSR in biocompatibility performance, depending on their chemistry.

MEDICAL EQUIPMENT MANUFACTURER S U R G I C A L X - R A Y G L A S S E S • Replace lead while providing uniform shielding performance • Radiation shielding up to 140KeV • Improve glasses design • Compliance with Radiation Protection Regulation: Adult eye exposure must be below 20 mSv per calendar year • Conducted extensive testing to ensure comparable and uniform shielding performance • Improved geometric flexibility • Lowered shielding component costs 30-50% by eliminating machining and assembly steps (associated with lead) • Reduced weight of the glasses and enabled a more ergonomic design • Eliminated disposal concerns associated with lead Trilliant™ XR Lead Replacement Thermoplastics KEY REQUIREMENTS WHY AVIENT? https://www.avient.com/products/engineered-polymer-formulations/conductive-signal-radiation-shielding-formulations/trilliant Medical equipment manufacturer

3 Certificate Certified sites according to appendix Scope concentrates and specialty compounds for the Healthcare and Medical device market. Normative basis EN ISO 13485:2016 Medical devices – Quality Management System Page 1 of 3 Appendix of main certificate H61173 Central function Scope Norm / Revision Reg. no.

Mevopur™ Healthcare Colorants and Formulations and Mevopur™ Healthcare Functional Additives for Bormed™ Resins Mevopur™ Healthcare Colorants and Formulations and Mevopur™ Healthcare Functional Additives help medical device, diagnostics and pharmaceutical packaging sectors meet the growing challenges of product consistency, compliance and reliability. 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.

Various materials and their resistnace to common disinfectants used in consumer, industrial, and medical applications 

Various materials and their resistnace to common disinfectants used in consumer, industrial, and medical applications 

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