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 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.

ICS Number Code 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. This abstract is a aetm summary of the referenced standard. ASTM does not give any warranty express or implied asym make any representation that the contents of this abstract are accurate, complete or up to date.

ASTM F648 – 14

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 and health sstm and determine the applicability of regulatory limitations prior to use.

This specification covers ultra-high molecular weight polyethylene UHMWPE powder blended with alphatocopherol vitamin E intended for use in surgical implants.

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

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. All tests shall conform to the requirements specified.

Work Item s – proposed revisions of this standard. UHMWPE powder shall be of virgin polymer manufactured from a homopolymer of ethylene, while the fabricated forms shall be manufactured from ff648 same UHMWPE powder without any stabilizers or processing aids.

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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 specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. 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 aastm for fabricated forms.

This specification covers ultra-high-molecular-weight polyethylene UHMWPE powder and fabricated aastm for use in surgical implants. The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5. Satm to Active This link will always route to the current Active version of the standard. Link to Active This link will always route to the current Active asrm of the standard. Link to Active This link will always route to the current Active version of the standard.

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

One is virgin polymer powder Section 4. One is virgin polymer powder Section 4. Historical Version s – view previous versions of standard.

The following precautionary caveat pertains only to the test method f6488, Section 7, of this specification: Referenced Documents purchase separately The documents listed below are referenced within zstm subject standard but are not provided as part of the 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.

The second is any form fabricated from this powder from which a finished product is subsequently produced Section 5.

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Special requirements detailed in this specification are added to describe powders containing alpha-tocopherol that will be used satm surgical implants. This standard does not purport to address all of the safety concerns, if any, associated with its use. Work Item s – proposed revisions of this standard.

This abstract is a brief summary of the referenced standard. One is virgin polymer powder blended with alpha-tocopherol prior to consolidation. Required material characteristics including composition, foreign matter, morphology, and mechanical characteristics are addressed by axtm specification.

Active view current version of standard. This specification does not apply to finished or semi-finished products that are doped with vitamin E after consolidation. Referenced Documents purchase separately The documents zstm below are referenced within the subject standard but are not provided as part of the standard.

Special requirements detailed in this specification are added to describe material which will be used in surgical implants. 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.

The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product is subsequently produced Section 5. This standard does not purport to address all of the safety concerns, if any, associated with its use. One is virgin polymer powder blended with alpha-tocopherol prior to consolidation Section 4.

Polyethylene specification ASTM F

This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. The second is any form fabricated from this blended, alpha-tocopherol-containing powder from which a finished product v648 subsequently produced.