ROSE Vice President, Corporate Communications Kyle Rose is Vice President, Corporate Communications, for Avient Corporation, the world’s premier provider of specialized and sustainable material solutions and services.

Cibodas Kecamatan Cibodas, Tangerang 15138 Indonesia Scope Category I Production of customer specific Masterbatches for Food packaging materials on the dedicated extrusion lines Normative base ISO 22000:2018 Food Safety Management Systems Requirements for any organization in the food chain Reg. no. 46391 Validity 25. 02. 2021 – 24. 02. 2024 Issue 30. 06. 2021 Swiss Madesqs.ch F.

SPORTS BRAND S N O R K E L M O U T H P I E C E • Replace PVC with alternative materials such as TPE or silicone • Skin contact safety and UV resistance • Soft texture with a non-sticky feel • Translucent color to help children use it properly and safely • Customized a soft (Shore A) TPE solution that passed strict tests, including thermal deformation (80°C for 2 hours), UV resistance, and assembly resistance • Providing a 40% more cost-effective system than silicone due to the high production efficiencies of TPEs • Provided cross-regional cooperation and prompt response to help customers achieve fast commercialization in both Europe and China Versaflex Thermoplastic Elastomers UV RESISTANT + TRANSLUCENT Copyright © 2025, Avient Corporation.

Our unique position in the supply chain allows us to work with suppliers to innovate materials solutions to help our customers succeed, while enabling a sustainable world. Use natural resources (e.g., water, sources of energy, raw materials) in an economical way. Inform Avient of financial, economic, supply changes (including origin or conflict status of 3TG metals), government regulations or other materials conditions that could affect ongoing operations or operating decisions, or if the company has been debarred as a government contractor

Precautions: the extruder should not be idle with the material in the hot barrel. Processing conditions can cause material properties to shift from the values stated in the information. Processing conditions can cause material properties to shift from the values stated in the information.

Plastisols will most likely change over time and material should be used on a first-in-first-out (FIFO) basis as quickly as possible. Processing conditions can cause material properties to shift from the values stated in the information. Stirring should be done gently so as not to introduce air or heat into the plastisol, but forceful enough to re-disperse any settled material on the bottom.

KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number, reducing risk of change • Non-phthalate and formulated without animal-derived substances • Color can be combined with additives to enhance performance and protection 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 Device Master File • Food contact established with FDA/EU* NOMINAL OUTSIDE DIAMETER OF NEEDLE (MM) COLOR DESCRIPTION RAL PANTONE TRANSPARENT PRODUCT CODE OPAQUE PRODUCT CODE 0.4 Medium Grey 7035 423 C PP7M665125 PP7M665127 0.45 Brown 8017 7588 C PP8M665294 PP8M665296 0.5 Orange 2003 173 C PP2M665298 PP2M665300 0.55 Medium Purple 4005 7676 C PP4M665290 PP4M665292 0.6 Deep Blue 5010 288 C PP5M665894 PP5M665896 0.7 Black 9005 Black C PP9M664950 PP9M664952 0.8 Deep Green 6001 7483 C PP6M665687 PP6M665689 0.9 Yellow 1021 115 C PP1M665211 PP1M665213 1.1 Cream 1015 7401 C PP0M665290 PP0M665292 1.2 Pink 3015 502 C PE3M665725 PP3M665727 Healthcare use limitations apply—see below. 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.

In order to satisfy the demand for a circular economy, governments are legislating increased use of recycled material in single use packaging. Our testing shows that ColorMatrix Amosorb 4020G is one of the most robust oxygen scavengers for PET rigid containers, with negligible effect on oxygen scavenging efficacy for the rPET grade tested, while other competitive materials lost almost all efficacy with rPET content as low as 20%. Processing conditions can cause material properties to shift from the values stated in the information.

KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified manufacturing sites, providing global consistency and increased security of supply • Documented change control beyond CAS number, reducing risk of change • Non-phthalate and formulated without animal- derived substances • Standard concentrates in a PE carrier and on request in PP • Pre-colored formulations can be supplied in specific resins selected for the application 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) • Food contact established with FDA/EU* APPLICATION BULLETIN DRUG TYPE COLOR DESCRIPTION PANTONE REFERENCE AVIENT PRODUCT CODE PE BASED Adrenergic agonist combinations Light Green 373 C PE6M176349 Adrenergic agonists Purple 2583 C PE4M176057 Anti-infectives Tan 467 C PE8M176130 Anti-inflammatory, nonsteroidal Grey Cool Grey 4 C PE7M176184 steroids Pink 197 C PE3M176237 Anti-inflammatory, immunomodulators Olive Green 5763 C On request Beta-blockers Yellow Yellow C PE1M176160 Beta-blocker combinations Dark Blue 281 C PE5M176272 Carbonic anhydrase inhibitors Orange 1585 C PE2M176089 Cytotoxic Black 6 C PL9M176008 Miotics Dark Green 348 C PE6M176267 Mydriatics and cycloplegics Red 1797 C PE3M176236 Prostaglandin analogues Turquoise 326 C PE5M176273 Healthcare use limitations apply—see below. 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.

VERSAFLEX™ VDT 4202-40B DYNAFLEX™ G7940-1 Application Anti-Vibration Feet Anti-Vibration Feet Defining Characteristic Vibration Damping Good Processability Compression Set Low Compression Set Low Compression Set Tactile Feel Grippy Feel Soft Touch, Rubbery Feel Coloring Black Natural Hardness 40 Shore A 40 Shore A Processing Injection Molding Injection Molding Overmolding Substrate Polypropylene Polypropylene HOW GLS TPEs MAKE THE DIFFERENCE IN HOME APPLIANCE ANTI-VIBRATION FEET • Reduced appliance movement and noise – vibration damping technology reduces movement and noise of the appliance when in use • Resistance to wear and tear – TPEs are proven to maintain their shape and resist tears with low compression set • Better performance and function – increase design freedom with material selection flexibility • Improved processability – boost efficiency with injection molding processing and reduce overall production cycle time and costs • Reduced number of part defects – eliminate secondary operations to achieve consistent and controlled results To learn more about GLS TPEs home appliances, visit www.avient.com or call +1.844.4AVIENT (1.844.428.4368). Processing conditions can cause material properties to shift from the values stated in the information. Processing conditions can cause material properties to shift from the values stated in the information.