2. These places may have varying supply chain demands and point of sale environments.

Document Page 2 of 10 Only the electronic version of this document in ETQ is the controlled version of the document. All packaged raw materials shall include the Avient raw material SAP code number and will not be compromised. Supplier containment shall take place without undue delay to avoid additional defective material shipment.

Customer collaboration and feedback has been extremely positive, and cultural integration has been excellent, as evidenced by the employee engagement scores that clearly reflect Avient is a great place to work. To participate in the audio-only portion of the call, dial 1-844-835-7433 (domestic) or 1-914-495-8589 (international) and provide conference ID number 3293155. To listen to this recording, dial 1-855-859-2056 (domestic) or 1-404-537-3406 (international) and provide conference ID number 3293155.

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.

KEY CHARACTERISTICS • Manufactured under ISO 13485 procedures • Documented change control beyond CAS number, reducing risk of change • Can be used on common injection molding and extrusion machines—set-up support by a technical assistance team • Available for use in polyolefins, styrenics and copolymers • Can be combined with colorants REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 - USP and (incl. class VI) - European Pharmacopeia, monograph 3.1.3/ 3.1.5 (polyolefin packaging materials) - USP (polyethylene) - Elemental impurities as per ICH Q3D • Registered Drug Master File (Type III) and/or Device Master File • Food contact according to USA FDA and EU norms APPLICATION BULLETIN Sustainability Spotlight Healthcare use limitations apply—see below. 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.

According to Filip Technologies, the FiLIP 2 uses cell tower location and Wi-Fi triangulation to supplement GPS data, which can more accurately pinpoint a child's location in areas where GPS is limited. Further enhancing its effectiveness, the FiLIP 2's cellular technology also enables parents and children to communicate with each other using two-way voice functionality to place and receive calls. We worked closely with Filip Technologies on this amazing new product, and we are very excited for the FiLIP 2 and its young customers," said Walter Ripple, vice president and general manager, for PolyOne's GLS business unit.

This will require a massive investment and deployment of smaller antennas and fiber optic cables strategically placed close together to deliver its intended performance," said Over the next decade as infrastructure is put in place, we expect double-digit revenue growth of our composite solutions, which includes 5G applications." High-frequency 5G networks rely on the densification of transmission antennae, resulting in an increased number of fiber optic cables and components capable of performing in harsh conditions. 

Existing, current MSDSs will continue to reside in our system for the time being, as we cannot convert all to the new format immediately. As new formulations are developed, the new format will be employed, and a GHS SDS will be generated and sent, replacing the previous MSDS in our system. By the deadline of June 2015 for North America and Europe, all MSDSs in these regions will have been converted to the new format SDS.

Usually, it is 2° for parallel walls. Holes are placed in a part for either structural support or cosmetic reasons. If the holes are not for structural design, they can be placed closer together and should all be placed two times the nominal wall thickness (W) apart from each other and from an outside or inside wall.

To participate in the audio-only portion of the call, dial 1-844-835- 7433 (domestic) or 1-914-495-8589 (international) and provide conference ID number 4774915. To listen to this recording, dial 1-855-859- 2056 (domestic) or 1-404-537-3406 (international) and provide conference ID number 4774915. They are based on management’s expectations that involve a number of business risks and uncertainties, any of which could cause actual results to differ materially from those expressed in or implied by the forward-looking statements.