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Standard Practice for Short-Term Screening of Implant Materials
Automatische name übersetzung:
Standard Praxis für Kurzzeit-Screening von Implantatmaterialien
NORM herausgegeben am 1.6.2010
Bezeichnung normen: ASTM F763-04(2010)
Anmerkung: UNGÜLTIG
Ausgabedatum normen: 1.6.2010
SKU: NS-56373
Zahl der Seiten: 4
Gewicht ca.: 12 g (0.03 Pfund)
Land: Amerikanische technische Norm
Kategorie: Technische Normen ASTM
Keywords:
biocompatibility, biomaterials, New Zealand white rabbits, orthopaedic medical devices, short-term implantation, tissue compatibility,Testing methods--surgical implants, Tissue reactions, New Zealand rabbits, Rabbits, Biocompatibility, Rapid screen test, Rats, Seals--surgical implant applications, Short term screening, Surgical implants, Test animals
Significance and Use | ||||||||||||||||||||||
The use of in vivo implantation techniques for characterizing the biocompatibility of materials to be utilized in various medical applications provides a unique assessment of such materials not achieved by other procedures. Physical characteristics (that is, form, density, hardness, surface finish) can influence the character of the tissue response to the test materials. This practice is intended as a rapid screening procedure for determining the acceptability of candidate materials. It would be invoked prior to using the long-term tests described in Practice F981. It is understood that for some applications additional tests, including long-term implantation studies, may be required to assess the final suitability of the candidate materials. This practice may not be appropriate for all types of implant applications. The user is cautioned to consider the appropriateness of the method in view of the materials being tested, their potential applications, and the recommendations contained in Practice F748. |
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1. Scope | ||||||||||||||||||||||
1.1 This practice provides guidelines for short-term testing or screening of candidate materials, both porous and dense, as to the effects of the material on animal tissue in which it is implanted. This is a rapid screening procedure for determining acceptability of candidate materials. 1.2 This practice, along with other appropriate biological tests (including other appropriate ASTM tests) may be used in the biocompatibility assessment of the candidate materials for use in the fabrication of devices for clinical application. 1.3 This experimental protocol is not designed to provide a comprehensive assessment of the systemic toxicity, carcinogenicity, teratogenicity, or mutagenicity of the material since other standards deal with these issues. 1.4 This practice is one of several developed for the assessment of the biocompatibility of materials. Practice F748 provides guidance for the selection of appropriate methods for testing materials for a specific application. 1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. |
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2. Referenced Documents | ||||||||||||||||||||||
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