1167302

ASTM F1635-95

Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants

standard by ASTM International , 01/01/1995

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Full Description

1.1 This test method covers poly(L-lactic acid) resin intended for use in surgical implants.

1.2 The requirements of this test method apply to poly(Llactic acid) in various forms:

1.2.1 Virgin polymer, or

1.2.2 Any form fabricated from virgin polymer such as a semi-finished component of a finished product, a finished product, which may include packaged and sterilized implants, or a specially fabricated test specimen.

 

Product Details

Published:
01/01/1995
Number of Pages:
4
File Size:
1 file , 23 KB
Note:
This product is unavailable in Russia, Ukraine, Belarus
 

Document History

  1. ASTM F1635-16


    Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants

    • Most Recent

  2. ASTM F1635-11


    Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants

    • Historical Version

  3. ASTM F1635-04a


    Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants

    • Historical Version

  4. ASTM F1635-04


    Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants

    • Historical Version

  5. ASTM F1635-95(2000)


    Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants

    • Historical Version

  6. ASTM F1635-95

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    Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants

    • Historical Version