ASTM F648 PDF

Polyethylene specification ASTM F Normative References. ASTM F Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and. Buy ASTM F SPECIFICATION FOR ULTRA-HIGH-MOLECULAR- WEIGHT POLYETHYLENE POWDER AND FABRICATED FORM. ASTM F Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants.

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This specification addresses material characteristics and does not apply to the r648 and sterilized finished implant. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. ICS Number Code The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product is subsequently produced Section 5.

ASTM F648 – 14

This specification covers ultra-high molecular weight polyethylene UHMWPE powder blended with alphatocopherol vitamin E intended for use in surgical implants. Historical Version s – view previous versions of standard. ICS Number Code This standard does not purport to address all of the safety concerns, if any, associated with its use. Link to Active This link will always route to the current Active version of the standard.

It is informational only and not an official part of the aatm the full text of the standard itself must be referred to for its use and application. The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5. One is virgin polymer powder blended with alpha-tocopherol prior to consolidation.

All tests shall conform to the requirements specified. 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.

This standard does not purport to address all of the safety concerns, if any, associated with its use. This specification does not apply to finished or semi-finished products that are doped with vitamin E after consolidation. Active view current version of standard. This standard does not purport to address all of the safety concerns, if any, associated with its use.

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This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard.

Required material characteristics including composition, foreign matter, morphology, and mechanical characteristics are addressed by this specification. One is virgin polymer powder Section 4. 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.

This specification does not apply to finished or semi-finished products that are doped with vitamin E after consolidation, nor to the packaged and sterilized finished implant, nor to UHMWPE materials extensively crosslinked by gamma and electron beam sources of ionizing radiation. The following precautionary caveat pertains only to the test method portion, Section 7, of this specification: ASTM does not give any warranty express or implied or make any representation that the contents of this abstract are accurate, complete or up to date.

Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. Work Item s – proposed revisions of this standard. Special requirements detailed in this specification are added to describe f6648 containing alpha-tocopherol that will be used in surgical implants.

This specification covers ultra-high-molecular-weight polyethylene UHMWPE powder and fabricated forms for use in surgical implants. UHMWPE powder shall be of virgin polymer manufactured from a homopolymer of ethylene, while the fabricated forms shall be manufactured from the same UHMWPE powder without any stabilizers or processing aids.

Tests for viscosity number, elongation stress, ash content, extraneous matter, and trace elements shall be performed for UHMWPE powders, while tests for density, ash content, tensile strength, yield strength, elongation, and impact strength shall be performed for fabricated forms. It is informational only and not an official part of the standard; the qstm text of the standard itself must be referred to for its use and application.

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ASTM does not give any warranty express or implied or make any representation that the contents of this abstract are accurate, complete or up to date. The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product is subsequently produced. 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 f6648 use.

Link to Active This link will always route to the current Active version of the standard. One is virgin polymer powder Section 4. Link to Active This link will always route to the current Active version of the standard. One is virgin polymer powder blended with alpha-tocopherol prior to consolidation Section 4.

Polyethylene specification ASTM F

Work Item s – proposed v648 of this standard. This specification also does not apply to UHMWPE materials extensively crosslinked by gamma and electron beam sources of ionizing radiation. This abstract is a brief summary of d648 referenced standard. The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5.

Special requirements detailed in this specification are added to describe material which will be used in surgical implants. This abstract is a brief summary of the referenced standard. This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. Historical Version s – view previous versions of standard.