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ISO 10993-18:2005
Biological evaluation of medical devices — Part 18: Chemical characterization of materials- 발행일 : 2005-06-30
- 발행기관 : ISO
상세정보
| 분야 | ISO/TC 194 : Biological and clinical evaluation of medical devices |
|---|---|
| 적용범위 | ISO 10993-18:2005 describes a framework for the identification of a material and the identification and quantification of its chemical constituents. The chemical characterization information generated can be used for a range of important applications, for example, as part of an assessment of the overall biological safety of a medical device (ISO 10993-1 and 14971), as a measurement of the level of a leachable substance in a medical device in order to allow the assessment of compliance with the allowable limit derived for that substance from health based risk assessment (ISO 10993-17), for judging equivalence of a proposed material to a clinically established material, for judging equivalence of a final device to a prototype device to check the relevance of data on the latter to be used to support the assessment of the former, or for screening of potential new materials for suitability in a medical device for a proposed clinical application. ISO 10993-18:2005 does not address the identification or quantification of degradation products, which is covered in ISO 10993-9, ISO 10993-13, ISO 10993-14 and ISO 10993-15. The ISO 10993 series of standards is applicable when the material or device comes into contact with the body directly or indirectly (see 4.2.1 of ISO 10993-1). ISO 10993-18:2005 is intended for suppliers of materials and manufacturers of medical devices, when carrying out a biological safety assessment. |
| 국제분류(ICS)코드 | 11.100.20 : 의료 장비의 생물학적 평가 |
| 페이지수 | 17 |
| Edition | 1 |
이력정보
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | ISO 10993-18:2020/Amd 1:2022상세보기 | Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process — Amendment 1: Determination of the uncertainty factor | 2022-05-11 | 표준 |
| 2 | ISO 10993-18:2020상세보기 | Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process | 2020-01-13 | 표준 |
| 3 | ISO 10993-18:2005상세보기 | Biological evaluation of medical devices — Part 18: Chemical characterization of materials | 2005-06-30 | 구판 |
| 4 | ISO/DIS 10993-18상세보기 | Biological evaluation of medical devices — Part 18: Chemical characterization of materials | 폐지 |
관련상품
- ISO/FDIS 10993-7 - Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals
- ISO/FDIS 10993-2 - Biological evaluation of medical devices — Part 2: Animal welfare requirements
- 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/DIS 10993-6 - Biological evaluation of medical devices — Part 6: Tests for local effects after implantation
다른 사람이 함께 구입한 상품
- ISO 10993-16:2017 - Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables
- ISO 10993-13:2010 - Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
- ISO 10993-4:2017 - Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
- ISO 10993-1:2018 - Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
- ISO 10993-17:2002 - Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
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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