DS/EN 60601-2-16/Corr.-2000

Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment

DS/EN 60601-2-16/Corr.-2000 发布历史

This articular standard specifies the minimum safety requirements for single patient haemodialysis, haemodiafiltration and haemofiltration equipment (as defined in 2.101). These devices are intended for use either by medical staff or under the supervision of medical expertise, including haemodialysis, haemodiafiltration and haemofiltration equipment operated by the patient.

DS/EN 60601-2-16/Corr.-2000由丹麦标准化协会 DK-DS 发布于 2000-10-09，并于 2000-06-23 实施。

DS/EN 60601-2-16/Corr.-2000在国际标准分类中归属于: 11.040.20 输血、输液和注射设备。

DS/EN 60601-2-16/Corr.-2000的历代版本如下：

• 2000年10月09日 DS/EN 60601-2-16/Corr.-2000

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标准号

DS/EN 60601-2-16/Corr.-2000

发布日期

2000年10月09日

实施日期

2000年06月23日

废止日期

无

国际标准分类号

11.040.20

发布单位

DK-DS

适用范围

This articular standard specifies the minimum safety requirements for single patient haemodialysis, haemodiafiltration and haemofiltration equipment (as defined in 2.101). These devices are intended for use either by medical staff or under the supervision of medical expertise, including haemodialysis, haemodiafiltration and haemofiltration equipment operated by the patient.