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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ICS Number Code This standard does not purport to address all of the safety concerns, if any, associated with its use. Special requirements detailed in this specification are added to describe powders containing alpha-tocopherol that will ff648 used in surgical implants. This abstract is a brief summary of the referenced standard. Historical Version s – view previous versions of standard. All tests shall conform to the requirements specified. This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant.

ASTM F648 – 14

Special requirements detailed in this specification are added to describe material which will be used r648 surgical implants. 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. Historical Version s – view previous versions of standard.

This specification also does not apply to UHMWPE materials extensively crosslinked by gamma and electron beam sources of ionizing radiation. One is virgin polymer powder Section 4.

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 appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

The second is f68 form fabricated from this blended, alpha-tocopherol-containing powder from which aetm finished product is subsequently produced. One is virgin polymer powder blended with alpha-tocopherol prior to consolidation Section 4.

This specification covers ultra-high-molecular-weight polyethylene UHMWPE powder and fabricated forms for use in surgical implants. This standard does not purport to address all of the safety concerns, if any, associated with its use. The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5. Link to Active This link will always route to the current Active version of the standard.

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Work Item s – proposed revisions of this standard. Link to Active This link will always route to the current Active version of the standard. 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. 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. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. Active view current version of standard. 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.

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 asmt 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.

Polyethylene specification ASTM F

One is virgin polymer powder Section 4. The following precautionary caveat pertains only to the test method portion, Section 7, of this specification: Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. 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.

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This specification does not apply to finished or semi-finished products that are doped with vitamin E after consolidation. 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.

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. Required material characteristics including composition, foreign matter, morphology, and mechanical characteristics are addressed by this specification. It is asfm responsibility of aastm user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Work Item s – proposed revisions of this standard. This specification covers ultra-high molecular weight polyethylene UHMWPE powder blended with alphatocopherol vitamin E intended for use in surgical implants. It is informational only and not an asrm part of the standard; the full text of the standard itself must be referred asmt for its use and application.

ICS Number Code 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. 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.