Avient Resources Avient Resources Learn more about our full portfolio of healthcare polymer solutions

Avient plays an important role in enhancing customer safety and has implemented internal GMP guidelines to help prevent products from being unintentionally adulterated.  Avient Canada ULC Avient Quality Policy

Covert Protection: These are methods that are hidden from the naked eye and only seen or apparent using special ID or testing equipment. These overt and covert technologies embed unique identification into the polymer the product is made from. Learn more about your anti-counterfeiting options by contacting an expert at Avient today!

As with all engineering and design, quality results from engineering simulation require the right capabilities, expertise, and experience. To learn more about FEA and how it can be applied to your polymer application, contact an expert at Avient today!

Under the Maxxam™ brand, standard grades are formulated with any combination of calcium carbonate, glass fiber, mica and talc to provide a desired balance of properties, including stiffness, durability, impact resistance and heat resistance. Some of the information arises from laboratory work with small-scale equipment which may not provide a reliable indication of performance or properties obtained or obtainable on larger-scale equipment. Processing conditions can cause material properties to shift from the values stated in the information.

Recommended mesh counts range from 25-40 th/in (10-15 th/cm).

These medical devices could benefit from the excellent chemical resistance found with Resilience™ HC Rigid Molding Materials Processing conditions can cause material properties to shift from the values stated in the information. When this improved chemical resistance is combined with excellent melt flow, flame resistance, UV resistance, and appearance, it’s easy to see why Resilience™ HC Rigid Molding Materials are becoming the materials of choice for rigid medical device housings.

Equipment maintenance: Maintaining plastisol mixing equipment up to industry standards may prove costly, and can require a significant amount of time from production operators.

China has been assessed and certified as meeting the requirements of 麟 ISO 13485:2016 EN ISO 13485:2016 ’骥鑫馨瓤） For the foiowing actratEes Design and manufacture of medical grade thermoplastic elastomers for non-active medical devices and active medical devices 遴；舞蒸；撇蒸 (non-implantable) ：护、：：于b入沙黔娜；舞睡莎：器器舞蟒檬非拟拐称群亘爸竺舀‘。 5‘冲」之七乃竿月 rf』J枯：“号淤，石 「3 ;:;This certificate is valid from 20 February 2021 until 19 February 2024 S SGSGS and remains valid subject to satisfactor y surveillance audits Re certification audit due before 6 January 2024 Issue 6.