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Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants
Automatische name übersetzung:
Standard-Spezifikation für ultra-hochmolekulares Polyethylen Pulver und Zeugform für chirurgische Implantate
NORM herausgegeben am 15.9.2010
Bezeichnung normen: ASTM F648-10
Anmerkung: UNGÜLTIG
Ausgabedatum normen: 15.9.2010
SKU: NS-56006
Zahl der Seiten: 9
Gewicht ca.: 27 g (0.06 Pfund)
Land: Amerikanische technische Norm
Kategorie: Technische Normen ASTM
Keywords:
fabricated forms, powdered form, ultra-high molecular weight polyethylene, Plastic surgical devices/applications--specifications, Polyethylene (PE) surgical implant applications--specifications, Powder coatings--specifications, UHMWPE (ultra-high molecular weight polyethylene), ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics), 83.080.20 (Thermoplastic materials)
1. Scope | ||||||||||||||||||||||||||||||||
1.1 This specification covers ultra-high molecular weight polyethylene powder (UHMWPE) and fabricated forms intended for use in surgical implants. 1.2 The requirements of this specification apply to UHMWPE in two forms. One is virgin polymer powder (Section 4). The second is any form fabricated from this powder from which a finished product is subsequently produced (Section 5). This specification addresses material characteristics and does not apply to the packaged and sterilized finished implant. 1.3 The requirements of this specification do not apply to UHMWPE virgin powder or fabricated forms intentionally crosslinked or blended with other additives, for example, antioxidents. 1.4 The biological response to polyethylene in soft tissue and bone has been well characterized by a history of clinical use (1, 2, 3) and by laboratory studies (4, 5, 6). 1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.6 The following precautionary caveat pertains only to the test method portion, Section 7, of this specification: 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 practices and determine the applicability of regulatory limitations prior to use. |
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2. Referenced Documents | ||||||||||||||||||||||||||||||||
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