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ISO 10993-9:2019
Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products- 발행일 : 2019-11-26
- 발행기관 : ISO
상세정보
분야 | ISO/TC 194 : Biological and clinical evaluation of medical devices |
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적용범위 | This document provides general principles for the systematic evaluation of the potential and observed degradation of medical devices through the design and performance of in vitro degradation studies. Information obtained from these studies can be used in the biological evaluation described in the ISO 10993 series. This document is applicable to both materials designed to degrade in the body as well as materials that are not intended to degrade. This document is not applicable to: a) the evaluation of degradation which occurs by purely mechanical processes; methodologies for the production of this type of degradation product are described in specific product standards, where available; NOTE Purely mechanical degradation causes mostly particulate matter. Although this is excluded from the scope of this document, such degradation products can evoke a biological response and can undergo biological evaluation as described in other parts of ISO 10993. b) leachable components which are not degradation products; c) medical devices or components that do not contact the patient's body directly or indirectly. |
국제분류(ICS)코드 | 11.100.20 : 의료 장비의 생물학적 평가 |
페이지수 | 11 |
Edition | 3 |
이력정보
No. | 표준번호 | 표준명 | 발행일 | 상태 |
---|---|---|---|---|
1 | ISO 10993-9:2019상세보기 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | 2019-11-26 | 표준 |
2 | ISO 10993-9:2009상세보기 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | 2009-11-30 | 구판 |
3 | ISO 10993-9:1999상세보기 | Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products | 1999-03-04 | 구판 |
4 | ISO/TR 10993-9:1994상세보기 | Biological evaluation of medical devices — Part 9: Degradation of materials related to biological testing | 1994-07-14 | 구판 |
관련상품
- ISO/FDIS 10993-2 - Biological evaluation of medical devices — Part 2: Animal welfare requirements
- ISO/DIS 10993-6 - Biological evaluation of medical devices — Part 6: Tests for local effects after implantation
- ISO/DIS 10993-3 - Biological evaluation of medical devices — Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity
- ISO/DIS 10993-18 - Biological evaluation of medical devices — Part 18: Chemical characterization of materials
- ISO/FDIS 10993-7 - Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals
다른 사람이 함께 구입한 상품
- ISO 10993-15:2019 - Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys
- ISO 10993-12:2021 - Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
- ISO 10993-18:2020 - Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
- ISO 14971:2019 - Medical devices — Application of risk management to medical devices
- ISO/TS 10993-19:2020 - Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials
추천 상품
- IEC TS 63134:2020 - Active assisted living (AAL) use cases
- IEC 60034-5:2020 RLV - Rotating electrical machines - Part 5: Degrees of protection provided by the integral design of rotating electrical machines (IP code) - Classification
- KS B ISO TS 25740-1 - 에스컬레이터 및 무빙워크에 대한 안전요건 — 제1부: 세계공통 필수 안전요건(GESRs)
- KS B ISO TS 8100-21 - 승객 및 화물 운송용 엘리베이터 —제21부: 세계공통 필수안전요건(GESRs)을 충족하는 세계공통 안전 파라미터(GSPs)
- KS C IEC TS 62872 - 산업 시설과 스마트 그리드 사이의 산업 공정 측정, 제어 및 자동화 시스템 인터페이스
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