Abstract

This part of IEC 60601 applies to the Basic Safety and Essential Performance of Transcutaneous Partial Pressure Monitors as defined in 201.3.203 hereinafter also referred to as ME- Equipment or ME-System. This document applies to Transcutaneous Partial Pressure Monitors intended for use in professional healthcare facilities in the Emergency Medical Service Environment or the Home Healthcare Environment.

Begin

2019-01-15

Planned document number

DIN EN IEC 60601-2-23

Project number

02228700

Responsible national committee

DKE/GUK 812.1 - Diagnostik und Brain Computer Interfaces  

Responsible international committee

ISO/TC 121/SC 3/JWG 14 - Joint ISO/TC 121/SC 3-IEC/SC 62D WG: Electromedical diagnostic and patient monitoring equipment  

draft standard

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment (IEC 62D/1627/CD:2018); Text in German and English
2019-05
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previous edition(s)

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:2011); German version EN 60601-2-23:2015
2016-08

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