https://www.avient.com/sites/default/files/resources/PDI_Case_Study_-_Medical_Device_0.pdf
The predictions
provided guidance in selecting the right temperatures to use
in a 30-day compressive creep test that enabled PDI to more
accurately estimate device performance over a 20-year span.
This
device exemplifies the next generation in disc replacement and offers mobility
equal to the body’s natural components.
CONTACT INFORMATION
Polymer Diagnostics Inc.
33587 Walker Road
Avon Lake, Ohio 44012
United States
+1 800 438 2335
+1 440 930 1644 fax
Polymer Diagnostics Inc. is a contract laboratory with accreditation to ISO/IEC 17025 by the
American Association for Laboratory Accreditation (A2LA) for both chemical and mechanical
capacities.
https://www.avient.com/resource-center?document_type=0&form_build_id=form-UG1SadN_IzwjaEoNv2mxi93WqDtETQ5gclbi1PCnUm0&form_id=resource_filter_form&industry=0&op=FILTER RESULTS&product_family=80&product_name=0&product_subfamily=0&page=1
Learn how Southern States Supplier used GlasArmor™ ballistic panels to protect electrical substations
Orthopedic Fixator Device
https://www.avient.com/resource-center?document_type=0&industry=0&product_family=80&product_subfamily=0&product_name=0&op=FILTER RESULTS&form_build_id=form-UG1SadN_IzwjaEoNv2mxi93WqDtETQ5gclbi1PCnUm0&form_id=resource_filter_form&page=1
Learn how Southern States Supplier used GlasArmor™ ballistic panels to protect electrical substations
Orthopedic Fixator Device
https://www.avient.com/investor-center/investor-news/archives?page=33
Tough Enough to Protect the Power Grid: Southern States LLC Selects GlasArmor™ Panels from PolyOne
CLEVELAND, June 20, 2016 /PRNewswire/ -- Southern States LLC, a Georgia manufacturer of products for the electric utility industry, recently selecte
https://www.avient.com/sites/default/files/2024-09/Avient_RY 2023 CDP Verification Opinion Declaration.pdf
VERIFICATION OPINION DECLARATION
GREENHOUSE GAS EMISSIONS
To: The Stakeholders of Avient Corporation
Apex Companies, LLC (Apex) was engaged to conduct an independent verification of the greenhouse gas (GHG)
emissions reported by Avient Corporation (Avient) for the period stated below.
Level of Assurance and Qualifications:
• Limited
• This verification used a materiality threshold of ±5% for aggregate errors in sampled data for each of the
above indicators
GHG Verification Methodology:
Evidence-gathering procedures included, but were not limited to:
• Interviews with relevant personnel of Avient and their consultant;
• Review of documentary evidence produced by Avient;
• Review of Avient data and information systems and methodology for collection, aggregation, analysis and
review of information used to determine GHG emissions; and
• Audit of sample of data used by Avient to determine GHG emissions.
It is our opinion that Avient has established appropriate systems for the collection, aggregation and analysis of
quantitative data for determination of these GHG emissions for the stated period and boundaries.
https://www.avient.com/sites/default/files/2023-01/Mevopur Healthcare Functional Additives_Laser Welding Additives for Medical Devices Application Bulletin.pdf
Mevopur™ Healthcare Functional Additives
Laser Welding Additives for Medical Devices
Laser welding has become a technology of choice
to join plastic parts of complex medical devices.
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.
https://www.avient.com/sites/default/files/2022-12/Mevopur Healthcare Colorants and Formulations_Functional Additives for IVD Devices Bulletin.pdf
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.
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.
https://www.avient.com/resources/safety-data-sheets?page=3652
140B MED GREY USIP1
https://www.avient.com/resources/safety-data-sheets?page=3767
457B SAND BEIGE USIP1
https://www.avient.com/resources/safety-data-sheets?page=3441
136B DK GREY USIP1