ASTM F2459 PDF

New ASTM F Standard Test Method for Extracting Residue from Metallic Medical Components and Quantifying via Gravimetric Analysis. ASTM F – Standard Test Method for Extracting Residue from. Metallic Medical Components and Quantifying via Gravimetric. Analysis. • ASTM F a baseline and set acceptance parameters for cleanliness. ASTM F Chemical Residue by. Gravimetric Analysis. This document provides a quantitative.

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This standard does not purport to address all of the safety concerns, if any, associated with its use.

Residues may also cause harm at locations away from the implant. Extractable residue includes aqueous and non-aqueous residue, as well as non-soluble residue. Print 1 astn 3 4 5 page sstarting from page current page.

Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the ast. Remember me for one month. This standard does not purport to address all of the safety concerns, if any, associated with its use.

It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

Residues may originate from manufacturing materials used in the course of processing or from the manufacturing environment, or may be the result of handling and packaging 1- 3. This practice proposes how to approach the identification of critical compounds and suggests different analytical methods.

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This test method is suitable for determination of the extractable residue in metallic medical components.

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ASTM-F, –

No other units of measurement are included in this standard. Work Item s – proposed revisions of this standard. This test method is also not intended to extract residue for use in biocompatibility testing. Search book title Enter keywords for book title search.

This test method is also not intended to extract residue for use in biocompatibility testing. In addition, it is recognized that this test method may not be the only method to determine and quantify extractables. 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.

Extractable residue includes aqueous and non-aqueous residue, as well as non-soluble residue. Register for a trial account. Enter your account email address to request a password reset: Link to Active This link will always route to the current Active version of the standard.

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New ASTM F Standard Test Method for Extracting Residue

Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. It identifies one technique to quantify extractable residue on metallic medical components. Copyright Compu-tecture, Inc. In addition, it is recognized that this test method may not be the only method to determine and quantify extractables.

Work Item s – proposed revisions of this standard. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. This test method is also not intended to extract residue for use in biocompatibility testing.

ASTM F2459 – 18

Link to Active This link will always route to the current Active version of the standard. Historical Version s – view axtm versions of standard. It identifies two techniques to quantify extractable residue on metallic medical components. If you like to setup a quick demo, let us know at support madcad.

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