This part of ISO 10993 provides general principles for the systematic evaluation of the potential and observed biode gradation of medical devices and for the design and performance of biodegradation studies.
This part of ISO 10993 is not applicable to:
(a) viable-tissue engineered products;
(b) methodologies for the generation of degradation products by mechanical processes. Methodologies for the production of this type of degradation product are described in specific product standards, where available;
(c) leachable components which are not degradation products.
Where product standards provide applicable product-specific methodologies for the identification and quantification of degrad ation products, those standards shall be considered as alternatives.
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Biological evaluation of medical devices -- Part 9: Degradation of materials rel
ated to biological testing (Adopted ISO/TR 10993-9:1994, first edition)