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EVS-EN 60601-2-16:2015

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

General information

Withdrawn from 03.06.2019
Base Documents
EN 60601-2-16:2015; IEC 60601-2-16:2012
Directives or regulations
None

Standard history

Status
Date
Type
Name
03.06.2019
Main
02.07.2015
Main
01.07.2001
Main
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as HAEMODIALYSIS EQUIPMENT. This International Standard does not take into consideration the DIALYSIS FLUID control system of HAEMODIALYSIS EQUIPMENT using regeneration of DIALYSIS FLUID and CENTRAL DELIVERY SYSTEMS. It does however take into consideration the specific safety requirements of such HAEMODIALYSIS EQUIPMENT concerning electrical safety and PATIENT safety. This International Standard specifies the minimum safety requirements for HAEMODIALYSIS EQUIPMENT. These devices are intended for use either by medical staff or for use by the PATIENT or other trained personnel under the supervision of medical expertise. This International Standard includes all ME EQUIPMENT that is intended to deliver a HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION treatment to a PATIENT suffering from kidney failure. The particular requirements in this International standard do not apply to: - EXTRACORPOREAL CIRCUITS; - DIALYSERS; - DIALYSIS FLUID CONCENTRATES; -  water treatment equipment; - equipment used to perform PERITONEAL DIALYSIS (see IEC 60601-2-39).

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