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NBR ISO 80601-2-12 : 2014

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS

Published date

09-02-2015

Superseded date

18-07-2025

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Committee
CB-026
DevelopmentNote
Supersedes NBR IEC 60601-2-12. (02/2015)
DocumentType
Standard
PublisherName
Brazilian Standards
Status
Superseded
SupersededBy

Standards Relationship
ISO 80601-2-12:2011 Identical

NBR ISO 5367 : 2017 ANAESTHETIC AND RESPIRATORY EQUIPMENT - BREATHING SETS AND CONNECTORS

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ISO 8836:2014 Suction catheters for use in the respiratory tract
ISO 7010:2011 Graphical symbols — Safety colours and safety signs — Registered safety signs
ISO 4871:1996 Acoustics — Declaration and verification of noise emission values of machinery and equipment
ISO 3744:2010 Acoustics — Determination of sound power levels and sound energy levels of noise sources using sound pressure — Engineering methods for an essentially free field over a reflecting plane
ISO 80601-2-13:2011 Medical electrical equipment — Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation
IEC 60068-2-27:2008 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
ISO 5356-1:2015 Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets
IEC 60068-2-31:2008 Environmental testing - Part 2-31: Tests - Test Ec: Rough handling shocks, primarily for equipment-type specimens
IEC 60068-2-64:2008 Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broadband random and guidance
ISO 10079-1:2015 Medical suction equipment — Part 1: Electrically powered suction equipment
ISO 32:1977 Gas cylinders for medical use — Marking for identification of content
ISO 5367:2014 Anaesthetic and respiratory equipment — Breathing sets and connectors
ISO 5359:2014 Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases
ISO 8185:2007 Respiratory tract humidifiers for medical use — Particular requirements for respiratory humidification systems
ISO 23328-2:2002 Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects
ISO 80601-2-55:2011 Medical electrical equipment — Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors
ISO 10079-3:2014 Medical suction equipment — Part 3: Suction equipment powered from a vacuum or positive pressure gas source
ISO 23328-1:2003 Breathing system filters for anaesthetic and respiratory use — Part 1: Salt test method to assess filtration performance
ISO 9360-1:2000 Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 1: HMEs for use with minimum tidal volumes of 250 ml
ISO 7000:2014 Graphical symbols for use on equipment — Registered symbols
ISO 9360-2:2001 Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml
ISO 10524-1:2006 Pressure regulators for use with medical gases — Part 1: Pressure regulators and pressure regulators with flow-metering devices
ISO 15223-1:2016 Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements
ISO 17664:2017 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices
ISO 7396-1:2016 Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum

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