• ASTM F 2848 : 2017 : REDLINE

    Current The latest, up-to-date edition.

    Standard Specification for Medical-Grade Ultra-High Molecular Weight Polyethylene Yarns

    Available format(s):  PDF

    Language(s):  English

    Published date:  01-05-2017

    Publisher:  American Society for Testing and Materials

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    Abstract - (Show below) - (Hide below)

    CONTAINED IN VOL. 13.01, 2017 Defines ultra-high molecular weight polyethylene (UHMWPE) yarns intended for use in medical devices or components of medical devices, such as sutures and ligament fixations.

    Scope - (Show below) - (Hide below)

    1.1This specification covers ultra-high molecular weight polyethylene (UHMWPE) yarns intended for use in medical devices or components of medical devices, such as sutures and ligament fixations. This specification covers natural (non-colored) and pigmented (colored) yarns.

    1.2This standard is intended to describe the requirements and the procedures to be followed for testing UHMWPE yarns as a component for medical devices prior to manufacturing processes of the medical device such as fabric formation, assembling and sterilization. This specification does not purport to address the requirements for the finished medical devices or the testing that is needed for medical devices that are fabricated from the components specified herein.

    1.3The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

    1.4This 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 practices and determine the applicability of regulatory limitations prior to use.

    TABLE 1 Requirements for UHMWPE Yarns

    Property

    Test Method

    Requirement

    Density, g/cm3

    Test Methods D792 or D1505

    0.95 - 1.00

    Melting temperature – peak, °C

    Test Method F2625

    140 - 150

    Filament Linear Density, dtex (Maximum)

    6.3

    2.7

    Intrinsic Viscosity, dl/g (Minimum)

    6.4

    15

    Tensile Strength, cN/dtex (Minimum)

    6.5

    26

    Tensile Modulus, cN/dtex (Minimum)

    6.5

    750

    Elongation-at-break, %

    6.5

    2 - 5

    Additional requirement for colored yarn:

     Pigment content, wt.% (Maximum)
     Chromium-cobalt-aluminum oxide

    6.2

    2

    1.5This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

    General Product Information - (Show below) - (Hide below)

    Committee F 04
    Document Type Redline
    Publisher American Society for Testing and Materials
    Status Current

    Standards Referenced By This Book - (Show below) - (Hide below)

    ASTM F 2027 : 2016 : REDLINE Standard Guide for Characterization and Testing of Raw or Starting Materials for Tissue-Engineered Medical Products

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 10993-4:2017 Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
    ASTM F 756 : 2017 : REDLINE Standard Practice for Assessment of Hemolytic Properties of Materials
    ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
    ASTM D 792 : 2013 : REDLINE Standard Test Methods for Density and Specific Gravity (Relative Density) of Plastics by Displacement
    ISO 2062:2009 Textiles Yarns from packages Determination of single-end breaking force and elongation at break using constant rate of extension (CRE) tester
    ISO 1628-3:2010 Plastics Determination of the viscosity of polymers in dilute solution using capillary viscometers Part 3: Polyethylenes and polypropylenes
    ISO 10993-18:2005 Biological evaluation of medical devices Part 18: Chemical characterization of materials
    ISO 10993-10:2010 Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
    ISO 10993-17:2002 Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
    ASTM F 748 : 2016 : REDLINE Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
    CFR 21(PTS1-99) : 0 FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 1-99
    ISO 14971:2007 Medical devices Application of risk management to medical devices
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