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ASTM F624-09
Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications
Automaticky přeložený název:
Standardní Příručka pro hodnocení z termoplastického polyuretanu, těles a řešení pro biomedicínské aplikace
NORMA vydána dne 1.8.2009
Informace o normě:
Označení normy: ASTM F624-09
Poznámka: NEPLATNÁ
Datum vydání normy: 1.8.2009
Kód zboží: NS-55936
Počet stran: 4
Přibližná hmotnost: 12 g (0.03 liber)
Země: Americká technická norma
Kategorie: Technické normy ASTM
Anotace textu normy ASTM F624-09 :
Keywords:
plastic surgical devices/applications, polymers-surgical applications, polyurethane-medical applications, Plastic surgical devices/applications, Polymers (surgical applications), Polyurethane--surgical applications, Thermoplastic surgical implant applications, ICS Number Code 11.120.01 (Pharmaceutics in general), 83.080.20 (Thermoplastic materials)
Doplňující informace
| Significance and Use | ||||||||||||||||||||||||||||||||||||||||||||||||
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This guide is intended to aid device fabricators in the selection of proper commercially available polyurethane solids and solutions for their application. The polyurethanes covered by this guide may be thermoformed or solution cast into biomedical devices for use as surgical aids or for implantation as determined to be appropriate, based on supporting biocompatibility and physical test data. |
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| 1. Scope | ||||||||||||||||||||||||||||||||||||||||||||||||
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1.1 This guide covers the evaluation of thermoplastic polyurethanes in both solid and solution form for biomedical applications. The polymers have been reacted to completion and require no further chemical processing. 1.2 The tests and methods listed in this guide may be referenced in specification containing minimum required values and tolerances for specific end-use products. 1.3 Standard tests for biocompatibility are included to aid in the assessment of safe utilization in biomedical applications. Compliance with these criteria shall not be construed as an endorsement of implantability. Since many compositions, formulations, and forms of thermoplastic polyurethanes in solid and solution forms are within this material class, the formulator or fabricator must evaluate the biocompatibility of the specific composition or form in the intended use and after completion of all manufacturing processes including sterilization. 1.4 Purchase specifications may be prepared by agreement between the buyer and seller by selection of appropriate tests and methods from those listed applicable to the specific biomedical end use. 1.5 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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