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IEC 60601-2-22:2007+AMD1:2012 CSV
Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment- 발행일 : 2012-10-26
- 발행기관 : IEC
- 대체표준 : IEC 60601-2-22:2019
상세정보
| 분야 | TC 76 : Optical radiation safety and laser equipment |
|---|---|
| 적용범위 | IEC 60601-2-22:2007+A1:2012 applies to the safety and essential performance of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as a class 3B or class 4 laser product as defined by 3.22 and 3.23 in IEC 60825-1, hereafter referred to as laser equipment. Throughout this International Standard, light emitting diodes (LED) are included whenever the word "laser" is used. This standard can also be applied to surgical, cosmetic, therapeutic and diagnostic laser equipment used for compensation or alleviation of disease, injury or disability. This third edition cancels and replaces the second edition of IEC 60601-2-22, published in 1995. This edition constitutes a technical revision. This third edition takes account of the recently published new editions of the General Standard IEC 60601-1 and publication IEC 60825-1. Additionally, it addresses technical and safety issues which have arisen in the time following the previous second edition. This consolidated version consists of the third edition (2007) and its amendment 1 (2012). Therefore, no need to order amendment in addition to this publication. |
| 국제분류(ICS)코드 |
31.260 : 광전자공학. 레이저 장비
11.040.50 : 방사선 및 기타 진단 기기 11.040.60 : 치료장비 |
| 페이지수 | 53 |
| Edition | 3.1 |
이력정보
| No. | 표준번호 | 표준명 | 발행일 | 상태 |
|---|---|---|---|---|
| 1 | IEC 60601-2-22:2019상세보기 | Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment | 2019-11-20 | 표준 |
| 2 | IEC 60601-2-22:2019 RLV상세보기 | Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment | 2019-11-20 | 표준 |
| 3 | IEC 60601-2-22:2007+AMD1:2012 CSV상세보기 | Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment | 2012-10-26 | 구판 |
| 4 | IEC 60601-2-22:2007/AMD1:2012상세보기 | Amendment 1 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment | 2012-10-25 | 구판 |
| 5 | IEC 60601-2-22:2007상세보기 | Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment | 2007-05-23 | 구판 |
| 6 | IEC 60601-2-22:1995상세보기 | Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment | 1995-11-08 | 구판 |
| 7 | IEC 60601-2-22:1992상세보기 | Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment | 1992-01-01 | 구판 |
관련상품
- IEC/DIS 60601-2-26 - Medical electrical equipment — Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs
- IEC 60601-2-15:1988 - Medical electrical equipment. Part 2: Particular requirements for the safety of capacitor discharge X-ray generators
- IEC 60601-2-14:1989 - Medical electrical equipment. Part 2: Particular requirements for the safety of electroconvulsive therapy equipment
- IEC 60601-2-32:1994 - Medical electrical equipment - Part 2: Particular requirements for the safety of associated equipment of X-ray equipment
- IEC 60601-1-4:1996 - Medical electrical equipment - Part 1: General requirements for safety - 4. Collateral standard: Programmable electrical medical systems
다른 사람이 함께 구입한 상품
- BS EN ISO 14971:2012 - Medical devices. Application of risk management to medical devices.
- ISO 14971:2007 - Medical devices — Application of risk management to medical devices
- ISO 14971:2019 - Medical devices — Application of risk management to medical devices
- IEC 60601-2-66:2015 - Medical electrical equipment - Part 2-66: Particular requirements for the basic safety and essential performance of hearing instruments and hearing instrument systems
- BS EN 60601-2-49:2015 - Medical electrical equipment. Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment.
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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