Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. 4. Buyer shall be exclusively responsible for (i) ensuring compliance with all Laws and Standards associated with its intended use of Product; and (ii) obtaining all necessary approvals, permits or clearances for such use. Buyer shall, upon demand by Seller, promptly return to Seller or destroy all such information.

All offers by Seller to sell Product are expressly conditioned on Buyer’s acceptance of these Terms. Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. 4. Buyer shall be exclusively responsible for (i) ensuring compliance with all Laws and Standards associated with its intended use of Product; and (ii) obtaining all necessary approvals, permits or clearances for such use.

Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. 4. Buyer shall be exclusively responsible for (i) ensuring compliance with all Laws and Standards associated with its intended use of Product; and (ii) obtaining all necessary approvals, permits or clearances for such use. Buyer shall, upon demand by Seller, promptly return to Seller or destroy all such information.

All offers by Seller to sell Product are expressly conditioned on Buyer’s acceptance of these Terms. Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. 4. Buyer shall be exclusively responsible for (i) ensuring compliance with all Laws and Standards associated with its intended use of Product; and (ii) obtaining all necessary approvals, permits or clearances for such use.

All offers by Seller to sell Product are expressly conditioned on Buyer’s acceptance of these Terms. Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. Buyer shall, upon demand by Seller, promptly return to Seller or destroy all such information.

Upon receipt of a notice of an alleged claim, Seller may suspend all further deliveries. 3. Buyer will comply with all Laws and Standards respecting the export and/or re-export of Product. Buyer shall be exclusively responsible for (i) ensuring compliance with all Laws and Standards associated with its intended use of Product; and (ii) obtaining all necessary approvals, permits or clearances for such use.

Customized color solutions are available on request • Production under ISO 13485 / GMP quality system with change control management • Fingerprinting of raw materials and routine batch testing • Extractability evaluated in hexane, isopropanol, and water according to ISO 10993 part 18 REGULATORY SUPPORT • Raw materials are pre-tested to biologically- evaluated raw materials using ISO 10993-1 and USP chapters , Class VI • DMF/MAF documentation filed with the FDA for all standard colors APPLICATIONS MEVOPUR LQ formulations can be applied in demanding applications including: • Medical devices such as catheter tubing & connectors, syringe tips, and needleless connectors • Skin contact devices such as wearables or soft-touch surfaces of medical devices PRODUCT BULLETIN MEVOPUR™-LQ YELLOW (PMS1205C) Product Code FZ1M415005 MEVOPUR™-LQ TRANS YELLOW Product Code FZ1M415006 MEVOPUR™-LQ BLUE (PMS292C) Product Code FZ5M415008 MEVOPUR™-LQ TRANS BLUE Product Code FZ5M415009 MEVOPUR™-LQ RED (PMS198C) Product Code FZ3M415008 MEVOPUR™-LQ TRANS RED Product Code FZ3M415009 MEVOPUR™-LQ GREEN (PMS346C) Product Code FZ6M415008 MEVOPUR™-LQ TRANS GREEN Product Code FZ6M415009 MEVOPUR™-LQ VIOLET (PMS2655C) Product Code FZ4M415003 MEVOPUR™-LQ TRANS VIOLET Product Code FZ4M415004 CUSTOM-MADE Individual options Customized colors are also available to meet your needs, please contact us. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product. 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, including the suitability of all raw materials and components used for its manufacture, and with all applicable laws and regulations. 1.844.4AVIENT www.avient.com

Because our system generates new SDS documents when there is a significant formulation or regulatory change, not all products will be accompanied by a new format SDS immediately. Existing, current MSDSs will continue to reside in our system for the time being, as we cannot convert all to the new format immediately. By the deadline of June 2015 for North America and Europe, all MSDSs in these regions will have been converted to the new format SDS.

KEY CHARACTERISTICS • Cost effective replacement for spray-on or painted frost effects • Easy dosing without secondary operations, which enhances maximum production efficiencies and provides sustainability • Better slip-resistant performance than normal PET bottle • Can be used in all ISBM molding machines TYPICAL USES SmartBatch Frost Collection can be used with all PET and adds premium value to customers. You have the responsibility to conduct full-scale end-product performance testing to determine suitability in your application, and you assume all risk and liability arising from your use of the information and/or use or handling of any product.

All nominees should be individuals of substantial accomplishment with demonstrated leadership capabilities. All such actions, interpretations and determinations that are done or made by the Board in good faith will be final, conclusive and binding. 2. Directors should regularly attend meetings of the Board and of all Board committees on which they serve.