1、 KS P ISO 10993 9KSKSKSKSSKSKSKS KSKSKS SKSKS KSKS SKS KS 9: KS P ISO 10993 9: 2007 (2012 ) 2007 10 31 http:/www.kats.go.krKS P ISO 10993 9: 2007 : ( ) ( ) () ( ) : (http:/www.standard.go.kr) : :2002 6 11 :2007 10 31 :2012 12 6 : 20120679 : ( 02-509-7294) (http:/www.kats.go.kr). 10 5 , . KS P ISO 10
2、993 9: 2007 i ii 1 1 2 1 3 .1 4 2 4.1 .2 4.2 .2 4.3 3 4.4 .3 5 .3 A( ) 5 B( ) .6 B.1 .6 B.2 6 B.3 6 8 KS P ISO 10993 9: 2007 ii 1999 1 ISO 10993 9, Biological evaluation of medical devices Part 9:Framework for identification and quantification of potential degradation products , . KS P ISO 10993 9:
3、2007 (2012 ) 9: Biological evaluation of medical devicesPart 9:Framework for identification and quantification of potential degradation products 1 . . a) b) . . c) , . 2 . . ( ) . KS P ISO 10993 1, 1: ISO 10993 2: 1992, Biological evaluation of medical devices Part 2: Animal welfare requirements 3 K
4、S P ISO 10993 1 . 3.1 (degradation) KS P ISO 10993 9: 2007 2 3.2 (biodegradation) . 3.3 (bioresorbable medical device) 3.4 (leachable) 3.5 (corrosion) . . 3.6 (substance) 3.7 (device component) . 3.8 (degradation product) 4 4.1 , , , . , , . (: KS P ISO 10993 13, KS P ISO 10990 14, KS P ISO 10993 15
5、). . 4.2 KS P ISO 10993 9: 2007 3 . , . . . A . . , , , , . KS P ISO 10993 1 . 4.3 4.1 . . a) , b) c) . / , . 4.4 , , . , , . , . B . . a) , b) c) , , d) 1 , , . 2 . 5 . KS P ISO 10993 9: 2007 4 a) , (B.1 ) b) c) (: , , , ) d) , , , e) f) GLP, ISO Guide 25 g) h) KS P ISO 10993 9: 2007 5 A ( ) . a) b
6、) 30 c) . a) , b) , c) . . (ISO 10993 2 ). , . KS P ISO 10993 9: 2007 6 B ( ) B.1 . . B.2 a) b) c) d) e) f) ( , ) g) h) i) j) k) l) m) B.3 B.3.1 , . . ( , ) B.3.2 . KS P ISO 10993 9: 2007 7 B.3.3 . ( ) KS P ISO 10993 9: 2007 8 1 KS P ISO 10993 13, 13: 2 KS P ISO 10993 14, 14: 3 KS P ISO 10993 15, 15
7、: 4 ISO Guide 25: 1990, General requirements for competence of calibration and testing laboratories 9: 153787 1 145 3(16) (02)26240114 (02)26240148 http:/ KS P ISO 10993 9: 2007KSKSKS SKSKS KSKS SKS KS SKS KSKS SKSKS KSKSKS Biological evaluation of medical devicesPart 9:Framework for identification and quantification of potential degradation products ICS 11.100 Korean Agency for Technology and Standards http:/www.kats.go.kr
copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1