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표준
판매
Medical electrical equipment. Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment.
| 분야 | |
|---|---|
| 적용범위 | Electronic equipment and components, Ultrasonic devices, Safety engineering, Medical equipment, Ultrasonic medical apparatus, Electrical safety, Electrical medical equipment, Performance, Clinical investigation instruments, Electrical equipment, Safety measures |
| 국제분류(ICS)코드 |
17.140.50 : 전자 음향
11.040.55 : 진단장비 |
| 페이지수 | 52 |
| Edition |
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | BS EN 60601-2-37:2008+A1:2015 | Medical electrical equipment. Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment. | 2015-09-30 | 표준 |
| 2 | BS EN 60601-2-37:2001 | Medical electrical equipment. Particular requirements for the safety of ultrasonic diagnostic and monitoring equipment. | 2006-06-30 | 폐지 |
BS EN 60601-2-17:1996 - Medical electrical equipment. Particular requirements for safety. Specification for remote-controlled automatically-driven gamma-ray afterloading equipment. 상세보기
BS EN 60601-2-2:1993 - Medical electrical equipment. Particular requirements for safety. Specification for high frequency surgical equipment. 상세보기
BS EN 60601-2-3:1993 - Medical electrical equipment. Particular requirements for safety. Specification for short-wave therapy equipment. 상세보기
BS EN 60601-1-1:1993 - Medical electrical equipment. General requirements for safety. Collateral standard. Safety requirements for medical electrical systems. 상세보기
BS EN 60601-2-22:1993 - Medical electrical equipment. Particular requirements for safety. Specification for diagnostic and therapeutic laser equipment. 상세보기
ISO 22301:2019 - Security and resilience — Business continuity management systems — Requirements 상세보기
IEC TR 62366-2:2016 - Medical devices - Part 2: Guidance on the application of usability engineering to medical devices 상세보기
BS EN ISO 14971:2019 - Medical devices. Application of risk management to medical devices. 상세보기
BS EN 62366-1:2015 - Medical devices. Application of usability engineering to medical devices. 상세보기
BS EN ISO 17664:2017 - Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. 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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