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Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices Corrigendum 1 to English version of DIN EN 556-1:2002-03
| 언어 | 제공형태 | 판매가격 | 선택 |
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| 국제분류(ICS)코드 | |
| 페이지수 | 2 |
| Edition |
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | DIN EN 556-1:2024-09 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2024 | 2024-09-01 | 표준 |
| 2 | DIN EN 556-1:2024-09 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | 2024-09-01 | 표준 |
| 3 | DIN EN 556-1:2023-02 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German and English version prEN 556-1:2023 | 2023-02-01 | 구판 |
| 4 | DIN EN 556-1 Berichtigung 1:2006-12 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001, Corrigenda to DIN EN 556-1:2002-03; German version EN 556-1:2001 | 2006-12-01 | 구판 |
| 5 | DIN EN 556-1 Berichtigung 1:2006-12 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices Corrigendum 1 to English version of DIN EN 556-1:2002-03 | 2006-12-01 | 구판 |
| 6 | DIN EN 556-1:2002-03 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001 | 2002-03-01 | 구판 |
| 7 | DIN EN 556-1:2002-03 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; English version of DIN EN 556-1 | 2002-03-01 | 구판 |
| 8 | DIN EN 556-1:2002-01 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001 | 2002-01-01 | 구판 |
DIN EN 556-2:2015-11 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices; German version EN 556-2:2015 상세보기
DIN EN 556-2:2015-11 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices 상세보기
DIN EN 556-2:2023-02 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: requirements for aseptically processed medical devices; German and English version prEN 556-2:2023 상세보기
DIN EN 556-1:2024-09 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2024 상세보기
DIN EN 556-1:2024-09 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices 상세보기
DIN EN 556-1:2002-03 - Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; English version of DIN EN 556-1 상세보기
BS EN ISO 13485:2016+A11:2021 - Medical devices. Quality management systems. Requirements for regulatory purposes. 상세보기
PD CEN/TR 17223:2018 - Guidance on the relationship between EN ISO 13485:2016 (Medical devices. Quality management systems. Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation. 상세보기
ASTM F1980-16 - Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices 상세보기
ASTM F88/F88M-15 - Standard Test Method for Seal Strength of Flexible Barrier Materials 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
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