ASTM D5227 PDF

This test method is a modification of the Food and Drug Administration FDA procedure for determining hexane extractables of polyolefins. This test method is based upon the presumption that the weight of the residue extract present in the solvent is equal to the amount extracted from the film sample and could therefore be quantified by measuring the weight loss of the extracted film, eliminating the complex and time-consuming evaporation process described in 21 CFR It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Units used in 21 CFR Multi-user access to over 3, medical device standards, regulations, expert commentaries and other documents.

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This test method is a modification of the Food and Drug Administration FDA procedure for determining hexane extractables of polyolefins. This test method is based upon the presumption that the weight of the residue extract present in the solvent is equal to the amount extracted from the film sample and could therefore be quantified by measuring the weight loss of the extracted film, eliminating the complex and time-consuming evaporation process described in 21 CFR It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Units used in 21 CFR Multi-user access to over 3, medical device standards, regulations, expert commentaries and other documents. Worldwide Standards We can source any standard from anywhere in the world. Learn more about the cookies we use and how to change your settings.

Online Tools. Search all products by. Plastics pipes and fittings. Implants for surgery. Ultra-high-molecular-weight polyethylene. Morphology assessment method. Click to learn more. Overview Product Details 1. Note 1 — There is no known ISO equivalent to this standard.

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ASTM D5227 - 13

Active view current version of standard. Other Historical Standards. Work Item s - proposed revisions of this standard. More D This test method is a modification of the Food and Drug Administration FDA procedure for determining hexane extractables of polyolefins. This test method is based upon the presumption that the weight of the residue extract present in the solvent is equal to the amount extracted from the film sample and could therefore be quantified by measuring the weight loss of the extracted film, eliminating the complex and time-consuming evaporation process described in 21 CFR It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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