Geon(TM) DB5334 Neutral Iso-Stable Shipment Notification - under "Material Header" MSDS - labeled as the "Product Number" (in Section 1)

Geon(TM)DB5291 NEUTRAL ISO STABLE BETTER HS Shipment Notification - under "Material Header" MSDS - labeled as the "Product Number" (in Section 1)

P1) ISO 3000Y Shipment Notification - under "Material Header" MSDS - labeled as the "Product Number" (in Section 1)

Get Help Now +1-866-737-2066 The PCF value of the TPEs was calculated using the ISO 14067:2018 standard and may be used as an input to determine the total greenhouse gas (GHG) emissions generated by a product over its entire life cycle.  

BIODÉGRADABLE ET COMPOSTABLE F I L M S D E P A I L L A G E • Conforme à la norme européenne EN17033 et certifiée OK Compost • Disponibles en noir ou blanc en standard avec différentes certifications TÜV Austria (OK Compost, etc • Prise en charge totale de la certification du produit final pour les normes EN13432 et EN17033 • Formulé avec des pigments testés et approuvés par un organisme certifié OnColor™ Bio-Colorants PRINCIPALES EXIGENCES POURQUOI AVIENT ?

ÍNDICE DE EPÍGRAFES SOLICITADOS: Datos Generales Situaciones Especiales DATOS GENERALES Indice AVIENT ESPAÑA SOCIEDAD LIMITADA 07/11/1983 Poligono Industrial, s/nºBARBASTRO22300-HUESCA Indefinida B22019723 EUID: ES22010.000000526 Hoja HU-2192 Tomo 494 Folio 6 La fabricacion y comercializacion de productos quimicos y auxiliares, tanto naturales como sinteticos, en relacion con las industrias del caucho, de resinas, de plasticos y de pinturas, y todas aquellas operaciones mercantiles que se relacionen con dicho objeto. En caso de discordancia prevalece el contenido de asientos registrales sobre el índice llevado por procedimientos informáticos.La Certificación expedida por el Registrador Mercantil será el único medio para acreditar fehacientemente el contenido de los asientos y demás documentos archivados o depositados en el Registro (Artículo 77 del Reglamento del Registro Mercantil).Queda totalmente prohibida la incorporación de los datos que se contienen en este documento a bases o ficheros informatizados que puedan ser susceptibles de consulta individualizada por personas físicas o jurídicas, y ello aunque se exprese la procedencia de la información (Instrucción DGRN de 17 de febrero de 1998).

1/1 Certification/Renovation Audit: 14-10-2022 Original approval date: - 1 Bureau Veritas Iberia S.L. Certificate Number: Certificate expiration date: Effective date: 31-10-2022 30-10-2025 Expiry date of previous cycle: 30-10-2022 31-10-2016 ES133794 Scope of certification: MANUFACTURING OF MASTERBATCHES, ADDITIVES AND COMPOUNDS FOR PIGMENTING THERMOPLASTIC MATERIALS USED IN FOOD INDUSTRY ISO 22000:2018 POLIGONO INDUSTRIAL EZCABARTE, C/H, Nº3 - 31194 - ORICAIN - NAVARRA - ESPAÑA AVIENT ESPAÑA, S.L.

KEY CHARACTERISTICS • Available for polyethylene, polypropylene, ABS, polycarbonate and styrenics • Bio-content of resin carrier varies from 70% to 100% depending on polymer—calculated to ASTM D6866 standard • Manufactured at four ISO 13485 certified sites, providing global consistency and security of supply • Documented change control beyond CAS number, reducing risk of change • Drop-in solutions that can be processed like fossil-based grades on common injection molding and extrusion machines • Can be provided as ready-to-use pre-colored or additive formulation 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 US FDA and APPLICATION BULLETIN Sustainability Spotlight Bio-polymers Healthcare use limitations apply—see below.

REGULATORY SUPPORT • Drug delivery devices • Pharmaceutical packaging • Medical equipment 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 the risk of change • Allows crystallization in semi-crystalline polymers to begin faster and complete earlier 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* APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below.

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 • Non-phthalate and formulated without animal-derived substances • Different tones of amber available on request —more or less red or yellow and/or lighter or darker • Also available in liquid form REGULATORY SUPPORT • Pre-tested raw materials: - ISO 10993-1 and USP parts (Class VI) - European Pharmacopeia, monograph 3.1.15, USP and elemental analysis as per ICH Q3D - USP criteria appearance of solution, color • Registered Drug Master File (Type III) by the FDA • Food contact compliance established with FDA/EU* • YBB00102002-2015 (oral liquid pharmaceutical PET bottles) compliance support APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below.