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BSI - BS EN ISO 80601-2-61

Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment

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Organization: BSI
Publication Date: 31 August 2011
Status: inactive
Page Count: 98
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

23/30451908 DC
September 11, 2023
Draft BS EN ISO 80601-2-61 Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
A description is not available for this item.
BS EN ISO 80601-2-61
February 28, 2019
Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
A description is not available for this item.
BS EN ISO 80601-2-61
February 28, 2019
Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
A description is not available for this item.
BS EN ISO 80601-2-61
August 31, 2011
Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
A description is not available for this item.

References

This document references:
NFPA 53 - Recommended Practice on Materials, Equipment, and Systems Used in Oxygen-Enriched Atmospheres
Published by NFPA on January 1, 2021
This document establishes recommended minimum criteria for the safe use of oxygen (liquid/gaseous) and the design of systems for use in oxygen and oxygen-enriched atmospheres (OEAs).
This document references:
IEC 60601-1 - MEDICAL ELECTRICAL EQUIPMENT – Part 1: General requirements for basic safety and essential performance
Published by IEC on March 1, 2021
A description is not available for this item.
This document references:
IEC 60721-3-7 - Classification of Environmental Conditions - Part 3-7: Classification of Groups of Environmental Parameters and Their Severities - Portable and Non-Stationary Use
Published by IEC on October 1, 2002
This standard classifies groups of environmental parameters and their severities to which products are subjected during portable and non-stationary use, including periods of transfer, down time,...
This document references:
93/42/EEC - Council Directive Concerning Medical Devices
Published by EU on June 14, 1993
Definitions, scope 1. This Directive shall apply to medical devices and their accessories. For the purposes of this Directive, accessories shall be treated as medical devices in their own right. Both...
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