CAN/CSA-C22.2 No.60601-2-4-2004(R2009)

Medical Electrical Equipment - Part 2-4: Particular Requirements for the Safety of Cardiac Defibrillators

CAN/CSA-C22.2 No.60601-2-4-2004(R2009) 发布历史

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)由SCC 发布于 2006-01-01。

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)在国际标准分类中归属于: 11.040.10 麻醉、呼吸和复苏设备。

CAN/CSA-C22.2 No.60601-2-4-2004(R2009) 的最新版本是哪一版？

最新版本是 CAN/CSA-C22.2 No.60601-2-4-2004(R2009) 。

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)的历代版本如下：

• 0000年 CAN/CSA-C22.2 No.60601-2-4-2004(R2009)

This National Standard of Canada is equivalent to International Standard IEC 60601-2-4:2002. 1 Scope and object This clause of the General Standard applies except as follows: *1.1 Scope Addition: This Particular Standard specifies requirements for the safety of CARDIAC DEFIBRILLATORS as defined in 2.1.101, hereinafter referred to as EQUIPMENT. This Particular Standard does not apply to implantable defibrillators, remote control DEFIBRILLATORS, external transcutaneous pacemakers, or separate stand alone CARDIAC MONITORS (which are standardized by IEC 60601-2-27). Cardiac monitors which use separate ECG monitoring electrodes are not within the scope of this standard unless they are used as the sole basis for AED rhythm recognition detection or beat detection for synchronized cardioversion. Defibrillation waveform technology is evolving rapidly. Published studies indicate that the effectiveness of waveforms varies. The choice of a particular waveform including waveshape, delivered energy, efficacy, and safety has been specifically excluded from the scope of this standard. However, due to the critical importance of the therapeutic waveform, comments have been added to the rationale which address considerations in waveform selection.

标准号

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)

发布

2006年

发布单位

SCC

当前最新

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)

 

 

代替标准

CAN/CSA-C22.2 No. 60601-2-4:12

被代替标准

CAN/CSA-C22.2 No.601.2.4-M90 (R2001)

CAN/CSA-C22.2 No.60601-2-4-2004(R2009)相似标准