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. This literature shall NOT operate as permission, recommendation, or inducement to practice any patented invention without permission of the patent owner. 1.844.4AVIENT www.avient.com RAL** SAP CODE DESCRIPTION LIGHT RESISTANCE 9010 CC01082068BG 00016 Cromofix White 8 1021 CC10253439BG PF 391-YE-30 FPVC Masterbatch 6 2003 CC10274055BG PF 274055 OR FPVC Masterbatch 5 3000 CC10253376BG PF 3189-RD-30 FPVC Masterbatch 4–5 3015 CC10255901BG PF 2000-PK-30 FPVC Masterbatch 7–8 4005 CC10255898BG PF 255898 PU FPVC Masterbatch 5 5015 CC10253374BG PF 130-BU-30 FPVC Masterbatch 7–8 6018 CC01088641BG 06B010 Cromofix Green 5–6 7001 CC10255354BG PF 255354 GY FPVC Masterbatch 8 8003 CC01088695BG 07B005 Cromofix Brown 6 9005 CC10252184BG PF 2023-BK-30 BK FPVC Masterbatch 8 * Non-ortho-phthalate plasticizers ** Other colors available on request SOLUTIONS AVAILABLE

Mevopur™ Healthcare Functional Additives Nucleating Agents Colors are used in the medical industry for brand recognition, the coding of different pharmaceuticals, or visual appeal. 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.

For the plastics used in these medical applications, this can mean compliance with the relevant chapters of the International Organization for Standardization (ISO), the United States Pharmacopeia Class VI (USP VI) the European Pharmacopeia (EP 3.1), and the International Conference on Harmonization (ICH Q3D) standards and guidelines.

For the plastics used in these medical applications, this can mean compliance with the relevant chapters of the International Organization for Standardization (ISO), the United States Pharmacopeia Class VI (USP VI) the European Pharmacopeia (EP 3.1), and the International Conference on Harmonization (ICH Q3D) standards and guidelines.

The state-of-the-art facility is strategically located in a hi-tech industrial park in the JinQiao Development Zone in Shanghai.

In addition to the two sites in Latin America, the company has four additional locations worldwide, including Merate (Italy), Singapore, and United States sites in West Chicago, Illinois, and Phoenix, Arizona.  

Certified for USP Class VI and ISO 10993, the new Versaflex HC BIO BT218 grade is manufactured in the United States with global commercial availability.  

The WO|Bone, manufactured in the United States, is available at www.wodesign.com and at select retailers.

QSR manufactures custom synthetic rubber components utilizing state-of-the-art automated liquid silicone molding as well as traditional transfer and compression molding processes.

EU Regulation No 528/2012 states that cable manufacturers in Europe can only use masterbatch additives that are authorized by BPR.