https://www.avient.com/company/sustainability/planet/lean-six-sigma
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https://www.avient.com/company/policies-and-governance/global-policy-antitrust
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https://www.avient.com/company/policies-and-governance/ethics-hotline
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https://www.avient.com/company/policies-and-governance-0/code-conduct
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https://www.avient.com/company/sustainability/performance/report-archive
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https://www.avient.com/company/sustainability/planet/responsible-care
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https://www.avient.com/news/specialty-healthcare-polymer-solutions-be-showcased-avient-mdm-west-2024
All Mevopur formulations are manufactured across a global network of ISO 13485 facilities, and they meet or exceed requirements for regulations such as USP Class VI, ISO 10993, USP 661, European Pharmacopeia, and ICH Q3D.
They are available in pre-colored or concentrate form in a range of vivid opaque and transparent colors that are fully bio-compatible per ISO 10993 standards.
https://www.avient.com/industries/healthcare/medical-devices-equipment/surgical-medical-instruments
Medical-grade colorant and functional additive masterbatches with robust bio-compatibility pre-testing to ISO, US Pharmacopeia, European Pharmacopeia, and ICH Q3D protocols to reduce risk, increase appeal, and boost performance
Soft-touch, durable, and colorable TPEs that comply with USP Class VI, ISO 10993, and ISO 9001 for diverse overmolding needs, aesthetics, and haptics
https://www.avient.com/sites/default/files/2025-03/ISO 13485 2025.pdf
Normative basis
EN ISO 13485:2016 Medical devices – Quality Management System
Reg. no.
EN ISO 13485:2016 H61173 01.03. 2025
29.02. 2028
Locations Scope Norm / Revision Reg. no.
EN ISO 13485:2016 H61173 01.03. 2025
29.02. 2028
Avient Colorants USA LLC
17 Foss Rd.
https://www.avient.com/company/sustainability/planet/environmental-stewardship/agency-support
Avient currently has twenty-three facilities globally certified to the Corporation’s GMP program and two facilities certified to "ISO 13485, Medical Device - Quality Management Systems - Requirements for Regulatory Purposes."
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