They are adapted to your manufacturing process and available as either a ‘ready-to-use’ formulation or a concentrate that is diluted in the Bormed™ resin of choice. 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 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. 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.

Field of application The manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber products for use in the public and private sectors.for use in the public and private sectors.for use in the public and private sectors.for use in the public and private sectors.

Certificate of Registration 9001:2015 MSP 9001:2015–MSP-ANAB-US (2.0) Page 1 of 2 Certificate of Registration of Quality Management System to ISO 9001:2015 The National Standards Authority of Ireland certifies that: Colorant Chromatics Ab Kroklundsvagen 346 AX-22 320 Odkarby Aland Finland has been assessed and deemed to comply with the requirements of the above standard in respect of the scope of operations given below: The Design, Manufacture and Sales of Fluoropolymer Color Concentrates and Compounds Additional sites covered under this multi-site certification are listed on the Annex (File No. 19.2540/C) Approved by: Geraldine LarkinChief Executive Officer Approved by: Lisa Greenleaf Operations Manager Registration Number: 19.2540/C Certification Granted: May 15, 1997 Effective Date: Oct 20, 2018 Expiry Date: Oct 19, 2021 National Standards Authority of Ireland, 20 Trafalgar Square, Nashua, New Hampshire, NH 03063, USA T +1 603 882 4412 9001:2015–MSP-ANAB-US (2.0) Page 2 of 2 Annex to Certificate Number: 19.2540/C Scope of Registration: The Design, Manufacture and Sales of Fluoropolymer Color Concentrates and Compounds Activity Location Central Management Group, Design, Manufacture Colorant Chromatics Kroklundsvagen 346 AX-22 320 Odkarby Aland Finland File No.: 19.2540/C Headquarters, Sales, Distribution Colorant Chromatics Europe B.V. Hastelweg 269 - 273 NL-5652 CV Eindhoven The Netherlands File No.: 19.2540/B Sales, Distribution Colorant GmbH Justus-Staudt-Strasse 1 Limburg-Offheim Germany 65555 File No.: 19.2540/A Design, Manufacture, Sales, Distribution Chromatics, Inc. 19 Francis J.

Field of application The manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber productsThe manufacturing and trading of synthetic fiber products for use in the public and private sectors.for use in the public and private sectors.for use in the public and private sectors.for use in the public and private sectors.

Virtual, computer-aided modelling is a critical tool to help predict part performance, streamline design, expedite prototyping and improve manufacturing efficiencies. If the simulation fails, parameters can be modified – enter a new material, modify the design, augment manufacturing, etc. – to yield the desired results. Hexagon’s Manufacturing Intelligence division provides solutions that use data from design and engineering, production and metrology to make manufacturing smarter.

A leading manufacturer/distributor in this market was faced with quality inconsistencies and supply availability issues with flat springs that were initially specified for their vibratory conveyors. With a high-heat flat spring option, manufacturers can potentially reduce overall conveyor system costs compared to higher priced coil spring systems. Made in the USA Avient’s Gordon Composites vibratory springs are manufactured in Montrose, Colorado using materials sourced from US suppliers.

The manufacturer was struggling to find a replacement material with excellent chemical resistance and a high flame retardant rating. Although PVC is one option, this manufacturer needed a colorable, drop-in replacement for PC/ABS. THE SOLUTION The manufacturer approached Avient with its challenge.

Mevopur™ Healthcare Functional Additives Chemical Foaming Agents (CFA) for Medical Devices and Pharmaceutical Packaging As the need to integrate sustainability in the design of healthcare products is growing, manufacturers of medical devices and pharmaceutical packaging are looking for materials with a more environmentally-friendly profile. They are specially formulated for healthcare applications and manufactured under controlled conditions. 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.

So HIVIZ product development engineers aimed their sights on recoil reduction technology for a major high-end rifle manufacturer, and it was game on. The new material, a GLS™ thermoplastic elastomer (TPE) from Avient, met the rigorous needs of the high-end rifle manufacturer, and then some. HIVIZ tests all manufactured products for a minimum of 10,000 rounds.