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Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)
| 분야 | |
|---|---|
| 적용범위 | |
| 국제분류(ICS)코드 | |
| 페이지수 | 76 |
| Edition |
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | DIN EN ISO 10993-23:2021-10 | Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021); German version EN ISO 10993-23:2021 | 2021-10-01 | 표준 |
| 2 | DIN EN ISO 10993-23:2021-10 | Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021) | 2021-10-01 | 표준 |
| 3 | DIN EN ISO 10993-23:2019-08 | Biological evaluation of medical devices - Part 23: Tests for irritation (ISO/DIS 10993-23:2019); German and English version prEN ISO 10993-23:2019 | 2019-08-01 | 구판 |
DIN EN ISO 10993-14:2009-08 - Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001); German version EN ISO 10993-14:2009 상세보기
DIN EN ISO 10993-14:2009-08 - Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) 상세보기
DIN EN ISO 10993-5:2009-10 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009); German version EN ISO 10993-5:2009 상세보기
DIN EN ISO 10993-5:2009-10 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) 상세보기
DIN EN ISO 10993-13:2010-11 - Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010); German version EN ISO 10993-13:2010 상세보기
DIN EN ISO 10993-12:2021-08 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021) 상세보기
DIN EN ISO 10993-18:2021-03 - Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020) 상세보기
DIN EN ISO 11737-2:2020-07 - Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019) 상세보기
DIN EN ISO 11137-1:2020-04 - Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd.1:2013 + Amd.2:2018) (includes Amendment A2:2019) 상세보기
DIN EN ISO 11135:2020-04 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019) 상세보기
IEC TS 63134:2020 - Active assisted living (AAL) use cases 상세보기
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 상세보기
KS B ISO TS 25740-1 - 에스컬레이터 및 무빙워크에 대한 안전요건 — 제1부: 세계공통 필수 안전요건(GESRs) 상세보기
KS B ISO TS 8100-21 - 승객 및 화물 운송용 엘리베이터 —제21부: 세계공통 필수안전요건(GESRs)을 충족하는 세계공통 안전 파라미터(GSPs) 상세보기
KS C IEC TS 62872 - 산업 시설과 스마트 그리드 사이의 산업 공정 측정, 제어 및 자동화 시스템 인터페이스 상세보기
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