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ASTM F648-00e1
Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants (Includes all amendments And changes 8/16/2017).
Automaticky preložený názov:
Štandardné špecifikácie pre Ultra - High - molekulovej hmotnosti prášku polyetylénu a kovových Formulár pre Chirurgické protézy
NORMA vydaná dňa 10.5.2000
Informácie o norme:
Označenie normy: ASTM F648-00e1
Poznámka: NEPLATNÁ
Dátum vydania normy: 10.5.2000
Kód tovaru: NS-56002
Počet strán: 8
Približná hmotnosť: 24 g (0.05 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Anotácia textu normy ASTM F648-00e1 :
Keywords:
fabricated forms, powdered form, ultra-high molecular weight polyethylene, ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics), 83.080.20 (Thermoplastic materials)
Doplňujúce informácie
| 1. Scope | ||||||||||||||||||||||||||||||||
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1.1 This specification covers ultra-high-molecular-weight polyethylene powder (UHMWPE) 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 provisions of Specification D4020 apply. Special requirements detailed in this specification are added to describe material which will be used in surgical implants. 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 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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