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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Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard.

The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product is subsequently produced Section 5. 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. One is virgin polymer powder Section 4. ICS Number Code One is virgin polymer powder blended with alpha-tocopherol prior to consolidation Section 4.

This abstract is a brief summary of the referenced standard. Active view current version of standard. The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product is subsequently produced. 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 This standard does not purport to address all of the safety concerns, if any, associated with its use.

Polyethylene specification ASTM F

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.

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. This specification also does not apply to UHMWPE materials extensively crosslinked by gamma and electron beam sources of ionizing radiation. It is the responsibility of the user of this standard to establish appropriate safety and health ast, and determine the applicability of regulatory limitations prior to use.

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This adtm does v648 apply to finished or semi-finished products that are doped with vitamin E after consolidation.

The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5. All tests shall conform to the requirements specified. This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. It is the responsibility of the user of this standard to establish f68 safety and health practices and determine the applicability of regulatory limitations prior to use.

ASTM F648 – 14

This specification covers ultra-high molecular weight polyethylene UHMWPE powder blended with alphatocopherol vitamin E intended for use in surgical implants. Link to Active This link will always route to the current Active version of ashm standard. Work Item s – proposed revisions of this standard. Work Item s – proposed revisions of this standard.

Required material characteristics including composition, foreign matter, morphology, and mechanical characteristics are addressed by this specification.

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 aztm strength shall be performed aetm fabricated forms. Link to Active This link will always route to the current Active version of the standard. This standard does not purport to address all of the safety concerns, if any, associated with its use.

This specification covers ultra-high-molecular-weight polyethylene UHMWPE powder and fabricated forms for use in surgical implants. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. Link to Active This link will always route to the current Active version of the standard.

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V648 specification ff648 material characteristics and does not apply to the packaged and sterilized finished implant. The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5.

Historical Asrm s – view previous versions of standard. Special requirements detailed in this specification are added to describe powders containing alpha-tocopherol that will be used in surgical implants. Special requirements detailed in this specification are aastm to describe material which will be used in surgical implants. Historical Version s – view previous versions of standard.

One is virgin polymer powder Section 4. 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.

This standard does not purport to address all of the safety concerns, if any, associated with its use. The following precautionary caveat pertains only to the test method portion, Section 7, of this specification: It is informational only and not an official part of the standard; the full text of the standard itself must be referred to for its use and application.

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 ast. It is informational only and not an official part of the standard; the full text of astn standard itself must be referred to for its use and application.