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.

Mobile Devices Inhalation Devices IVD Devices

Inhalation Devices IVD Devices Medical Devices & Equipment

Mobile Devices Inhalation Devices IVD Devices

MEVOPUR™ Special Effects for Healthcare Devices and Pharmaceutical Packaging - Application Bulletin (Chinese) Liquid color & additive concentrates designed for use in medical devices and pharmaceutical packaging Mevopur™ Bio-Based Polymer Solutions for Medical Devices and Pharmaceutical Packaging (Japanese)

MEVOPUR™ Special Effects for Healthcare Devices and Pharmaceutical Packaging - Application Bulletin (Chinese) Liquid color & additive concentrates designed for use in medical devices and pharmaceutical packaging Mevopur™ Bio-Based Polymer Solutions for Medical Devices and Pharmaceutical Packaging (Japanese)

Mobile Devices Inhalation Devices IVD Devices

Normative basis EN ISO 13485:2016 Medical devices – Quality Management System Reg. no. Ltd. 30, Hsing Pang Road 33068 Taoyuan Taiwan Design and manufacture of colour and additive concentrates and specialty compounds for the Healthcare and Medical device market. Lewiston, ME, 04240 United States of America Design and manufacture of colour and additive concentrates and specialty compounds for the Healthcare and Medical device market.

Comprehensive consulting and testing expertise for medical materials and device companies Committed to Growing with the Medical Industry Since 2009, PDI has invested over $2 million to improve and extend our capabilities to serve our medical materials and device clients. PDI) is a complete solutions provider of plastics testing and polymer consulting within the medical materials and device industries. Comprehensive consulting and testing expertise for medical materials and device companies Committed to Growing with the Medical Industry Since 2009, PDI has invested over $2 million to improve and extend our capabilities to serve our medical materials and device clients.

Microsoft Word - AvientRY 2021 CDP Verification Opinion Declaration_07-26-22r WATER RESOURCES • ENVIRONMENTAL SERVICES • HEALTH & SAFETY • CLIMATE CHANGE Apex Companies, LLC • (800) 733-2739 • www.apexcos.com VERIFICATION OPINION DECLARATION GREENHOUSE GAS EMISSIONS To: The Stakeholders of Avient Corporation Apex Companies, LLC (Apex) was engaged to conduct an independent verification of the greenhouse gas (GHG) emissions reported by Avient Corporation (Avient) for the period stated below. Level of Assurance and Qualifications:  Limited  This verification used a materiality threshold of ±5% for aggregate errors in sampled data for each of the above indicators GHG Verification Methodology: Evidence-gathering procedures included, but were not limited to:  Interviews with relevant personnel of Avient and their consultant;  Review of documentary evidence produced by Avient;  Review of Avient data and information systems and methodology for collection, aggregation, analysis and review of information used to determine GHG emissions; and  Audit of sample of data used by Avient to determine GHG emissions. It is our opinion that Avient has established appropriate systems for the collection, aggregation and analysis of quantitative data for determination of these GHG emissions for the stated period and boundaries.