Through their close work with amputees from all five activity levels of the MFCL system, the team at WillowWood recognized that prosthetic options were limited for K2 amputees who are able to handle more uneven surfaces. And it does all of this in an updated, attractive design. © 2020, All Rights Reserved Avient Corporation, 33587 Walker Road, Avon Lake, Ohio USA 44012

CESA™ Antimicro Additives Antimicrobial PRODUCT SELECTION GUIDE Microorganisms like fungi and bacteria are present in all environments. All CESA Antimicro products are manufactured in an EPA-registered facility. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product.

You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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.

Drop all heating sections 50°F–100°F during extended downtime, die changes, etc. or keep bleeding if possible. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product.

Carbon Black is by far the most important black pigment, and is the second most used in terms of volume of all pigments employed by the plastic industry, ranking behind only TiO2. Environment In accordance with all local legislation and permit requirements. Elemental Carbon is widely distributed in nature and is an essential element in the components of all living organisms.

While these are all good ways to improve a package’s sustainability, they aren’t without their challenges. These may include: • Achieve a percentage of all packaging that is reusable, recyclable or compostable • Increase the use of post-consumer recycled (PCR) content, up to 100% • Use lightweighting or other solutions that will help reduce your carbon footprint • Replace petroleum-based materials with renewable materials such as bio-plastics Whatever your goals, we can help you achieve them with customized solutions based on a number of factors. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product.

You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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.

You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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

You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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.

You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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.