December 30, 2016

U KAS MANAC〔M〔N丁 SYSTEMS 0005 、端；薰；; HCSGS 13485 2016 Olin ：氨 城心〔找n心亡〔 ．．八 护、产、八 j 丹月六户 八八月户 八月月‘、 ）如》 称资熨面蔚若三 「｛羹 StS55G S GSlfS5SG56SGSGSGSGSGSG5G5 f5 嚷i羹羹巍熊燕鬓；；奎忿 rage I Oil;；燕七 :终 sds 0Gs、 山5互 0s's""“ 刀之： J"‘、 ,slttiGsti.' 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‘。

July 26, 2016 July 26, 2016

February 3, 2016 Feb. 3, 2016

February 3, 2016 Feb. 3, 2016

To support this, Avient’s medical-grade colorants and additives are manufactured at sites certified under GMP or ISO 13485-2016 standards. They are manufactured at an ISO13485-2016-certified site and pre-tested to specific regulatory demands, including USP Class VI and ISO 10993.

2 /J u n -2 0 1 9 /V er si o n 1 .0 Certificate Avient Colorants Singapore Pte Ltd 8 Third Chin Bee Road Jurong Industrial Estate 618684 Singapore Singapore Scope Administration, Site management, Manufacture, Laboratory, Procurement, Maintenance, infrastructure, Warehouse and Transport Normative base EN ISO 13485:2016 Medical devices – Quality Management System Reg. no. 45483 Validity 01. 03. 2022  – 28. 02. 2025 Issue 01. 03. 2022  A.Grisard, President SQS F.

in 2013 as president of Performance Products & Solutions (PP&S), where he served until his appointment to chief commercial officer in 2016. 

MEVOPUR medical-grade materials are produced according to ISO13485-2016 protocols and supported by testing to ISO 10993-1, USP, European Pharmacopeia and ICH Q3D guidelines.

with 2016 revenues of