Filter :
| Standard and/or project under the direct responsibility of ISO/TC 121/SC 3 Secretariat | Stage | ICS |
|---|---|---|
|
ISO 5369:1987 [Withdrawn]
Breathing machines for medical use — Lung ventilators
|
95.99 | |
|
ISO 7767:1988 [Withdrawn]
Oxygen analyzers for monitoring patient breathing mixtures — Safety requirements
|
95.99 | |
|
ISO 8185:1988 [Withdrawn]
Humidifiers for medical use — Safety requirements
|
95.99 | |
|
ISO 8185:1997 [Withdrawn]
Humidifiers for medical use — General requirements for humidification systems
|
95.99 | |
|
ISO 8185:1997/Cor 1:2001 [Withdrawn]
Humidifiers for medical use — General requirements for humidification systems — Technical Corrigendum 1
|
95.99 | |
|
ISO 8185:2007 [Withdrawn]
Respiratory tract humidifiers for medical use — Particular requirements for respiratory humidification systems
|
95.99 | |
|
ISO 8359:1988 [Withdrawn]
Oxygen concentrators for medical use — Safety requirements
|
95.99 | |
|
ISO 8359:1996 [Withdrawn]
Oxygen concentrators for medical use — Safety requirements
|
95.99 | |
|
ISO 8359:1996/Amd 1:2012 [Withdrawn]
Oxygen concentrators for medical use — Safety requirements — Amendment 1
|
95.99 | |
|
ISO 8382:1988 [Withdrawn]
Resuscitators intended for use with humans
|
95.99 | |
|
ISO 9360:1992 [Withdrawn]
Anaesthetic and respiratory equipment — Heat and moisture exchangers for use in humidifying respired gases in humans
|
95.99 | |
|
ISO 9703-1:1992 [Withdrawn]
Anaesthesia and respiratory care alarm signals — Part 1: Visual alarm signals
|
95.99 | |
|
ISO 9703-2:1994 [Withdrawn]
Anaesthesia and respiratory care alarm signals — Part 2: Auditory alarm signals
|
95.99 | |
|
ISO 9703-3:1998 [Withdrawn]
Anaesthesia and respiratory care alarm signals — Part 3: Guidance on application of alarms
|
95.99 | |
|
ISO 9919:1992 [Withdrawn]
Pulse oximeters for medical use — Requirements
|
95.99 | |
|
ISO 9919:2005 [Withdrawn]
Medical electrical equipment — Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use
|
95.99 | |
|
ISO 10651-1:1993 [Withdrawn]
Lung ventilators for medical use — Part 1: Requirements
|
95.99 | |
|
ISO 10651-2:1996 [Withdrawn]
Lung ventilators for medical use — Part 2: Particular requirements for home care ventilators
|
95.99 | |
|
ISO 10651-2:2004 [Withdrawn]
Lung ventilators for medical use — Particular requirements for basic safety and essential performance — Part 2: Home care ventilators for ventilator-dependent patients
|
95.99 | |
|
ISO 10651-3:1997 [Withdrawn]
Lung ventilators for medical use — Part 3: Particular requirements for emergency and transport ventilators
|
95.99 | |
|
ISO 10651-4:2002 [Withdrawn]
Lung ventilators — Part 4: Particular requirements for operator-powered resuscitators
|
95.99 | |
|
Lung ventilators — Part 4: Particular requirements for user-powered resuscitators
|
60.60 | |
|
Lung ventilators for medical use — Particular requirements for basic safety and essential performance — Part 5: Gas-powered emergency resuscitators
|
90.60 | |
|
ISO 10651-6:2004 [Withdrawn]
Lung ventilators for medical use — Particular requirements for basic safety and essential performance — Part 6: Home-care ventilatory support devices
|
95.99 | |
|
Medical electrical equipment — Clinical performance evaluation of clinical thermometers
|
60.60 | |
|
ISO/TR 13154:2009 [Withdrawn]
Medical electrical equipment — Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph
|
95.99 | |
|
Medical electrical equipment — Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph
|
60.60 | |
|
ISO 17510-1:2002 [Withdrawn]
Sleep apnoea breathing therapy — Part 1: Sleep apnoea breathing therapy devices
|
95.99 | |
|
ISO 17510-1:2002/Cor 1:2004 [Withdrawn]
Sleep apnoea breathing therapy — Part 1: Sleep apnoea breathing therapy devices — Technical Corrigendum 1
|
95.99 | |
|
ISO 17510-1:2007 [Withdrawn]
Sleep apnoea breathing therapy — Part 1: Sleep apnoea breathing therapy equipment
|
95.99 | |
|
ISO 17510-2:2003 [Withdrawn]
Sleep apnoea breathing therapy — Part 2: Masks and application accessories
|
95.99 | |
|
ISO 17510-2:2007 [Withdrawn]
Sleep apnoea breathing therapy — Part 2: Masks and application accessories
|
95.99 | |
|
ISO 17510:2015 [Withdrawn]
Medical devices — Sleep apnoea breathing therapy — Masks and application accessories
|
95.99 | |
|
Medical devices — Sleep apnoea breathing therapy — Masks and application accessories
|
60.60 | |
|
ISO 18562-1:2017 [Withdrawn]
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
|
95.99 | |
|
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
|
60.60 | |
|
ISO 18562-2:2017 [Withdrawn]
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 2: Tests for emissions of particulate matter
|
95.99 | |
|
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 2: Tests for emissions of particulate matter
|
60.60 | |
|
ISO 18562-3:2017 [Withdrawn]
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic compounds (VOCs)
|
95.99 | |
|
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic substances
|
60.60 | |
|
ISO 18562-4:2017 [Withdrawn]
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate
|
95.99 | |
|
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate
|
60.60 | |
|
ISO 18778:2005 [Withdrawn]
Respiratory equipment — Infant monitors — Particular requirements
|
95.99 | |
|
Respiratory equipment — Particular requirements for basic safety and essential performance of infant cardiorespiratory monitors
|
60.60 | |
|
ISO 18779:2005 [Withdrawn]
Medical devices for conserving oxygen and oxygen mixtures — Particular requirements
|
95.99 | |
|
Anaesthetic and respiratory equipment — Passive humidifiers
|
90.93 | |
|
Guidance on the selection of the appropriate means of ventilation based on the intended patient, use environment, and operator
|
60.60 | |
|
ISO 23747:2007 [Withdrawn]
Anaesthetic and respiratory equipment — Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans
|
95.99 | |
|
Anaesthetic and respiratory equipment — Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans
|
90.93 | |
|
Anaesthetic and respiratory equipment — Spirometers intended for the measurement of time forced expired volumes in humans
|
90.92 | |
|
Anaesthetic and respiratory equipment — Spirometers intended for the measurement of time forced expired volumes in humans — Technical Corrigendum 1
|
60.60 | |
|
ISO/CD 26782 [Under development]
Anaesthetic and respiratory equipment — Spirometers intended for the measurement of time forced expired volumes in humans
|
30.99 | |
|
Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral standard: Requirements for the development of physiologic closed-loop controllers
|
90.92 | |
|
IEC 60601-1-11:2010 [Withdrawn]
Medical electrical equipment — Part 1-11: General requirements for basic safety and essential performance — Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
|
95.99 | |
|
Medical Electrical Equipment — Part 1-12: General requirements for basic safety and essential performance — Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the emergency medical services environment
|
90.60 | |
|
IEC 60601-1-8:2003 [Withdrawn]
Medical electrical equipment — Part 1-8: General requirements for safety — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
|
95.99 | |
|
Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral standard: Requirements for the development of physiologic closed-loop controllers — Amendment 1
|
60.60 | |
|
IEC 60601-1-11:2010/Cor 1:2011 [Withdrawn]
Medical electrical equipment — Part 1-11: General requirements for basic safety and essential performance — Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment — Technical Corrigendum 1
|
95.99 | |
|
Medical Electrical Equipment — Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the emergency medical services environment — Amendment 1
|
60.60 | |
|
IEC 60601-1-8:2003/Amd 1:2006 [Withdrawn]
Medical electrical equipment — Part 1-8: General requirements for safety — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems — Amendment 1
|
95.99 | |
|
Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral standard: Requirements for the development of physiologic closed-loop controllers — Amendment 2
|
60.60 | |
|
IEC/AWI 60601-1-10 [Under development]
Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral standard: Requirements for the development of physiologic closed-loop controllers
|
20.00 |
|
|
Medical electrical equipment — Part 1-11: General requirements for basic safety and essential performance — Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
|
90.93 | |
|
Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
|
90.60 | |
|
IEC 60601-2-12:2001 [Withdrawn]
Medical electrical equipment — Part 2-12: Particular requirements for the safety of lung ventilators — Critical care ventilators
|
95.99 | |
|
Medical electrical equipment — Part 1-11: General requirements for basic safety and essential performance — Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment — Amendment 1
|
60.60 | |
|
Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems — Amendment 1
|
60.60 | |
|
Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems — Amendment 2
|
60.60 | |
|
ISO 80601-2-90:2021 [Withdrawn]
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment
|
95.99 | |
|
ISO/AWI 80601-2-96 [Under development]
Medical electrical equipment — Part 2-96: Particular requirements for basic safety and essential performance of non-invasive arterial tonometer equipment
|
20.00 |
|
|
ISO/AWI 80601-2-97 [Under development]
Medical electrical equipment — Part 2-97: Particular requirements for basic safety and essential performance of supportive home high-flow respiratory equipment
|
20.00 |
|
|
Medical electrical equipment — Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs
|
90.93 | |
|
IEC 80601-2-30:2009 [Withdrawn]
Medical electrical equipment — Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers
|
95.99 | |
|
Medical electrical equipment — Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment
|
90.60 | |
|
IEC 80601-2-59:2008 [Withdrawn]
Medical electrical equipment — Part 2-59: Particular requirements for basic safety and essential performance of screening thermographs for human febrile temperature screening
|
95.99 | |
|
IEC 80601-2-71:2015 [Withdrawn]
Medical electrical equipment — Part 2-71: Particular requirements for the basic safety and essential performance of functional Near-Infrared Spectroscopy (NIRS) equipment
|
95.99 | |
|
IEC/DIS 80601-2-23 [Under development]
Medical electrical equipment — Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
|
40.60 | |
|
IEC/DIS 80601-2-86 [Under development]
Medical electrical equipment — Part 2-86: Particular requirements for the basic safety and essential performance of electrocardiographs, including diagnostic equipment, monitoring equipment, ambulatory equipment, electrodes, cables and leadwires
|
40.00 | |
|
ISO 80601-2-12:2011 [Withdrawn]
Medical electrical equipment — Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
|
95.99 | |
|
ISO 80601-2-56:2009 [Withdrawn]
Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
|
95.99 | |
|
ISO 80601-2-61:2011 [Withdrawn]
Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
|
95.99 | |
|
ISO 80601-2-67:2014 [Withdrawn]
Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment
|
95.99 | |
|
ISO 80601-2-69:2014 [Withdrawn]
Medical electrical equipment — Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment
|
95.99 | |
|
ISO 80601-2-70:2015 [Withdrawn]
Medical electrical equipment — Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment
|
95.99 | |
|
ISO 80601-2-72:2015 [Withdrawn]
Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients
|
95.99 | |
|
ISO 80601-2-74:2017 [Withdrawn]
Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
|
95.99 | |
|
ISO 80601-2-79:2018 [Withdrawn]
Medical electrical equipment — Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
|
95.99 | |
|
ISO 80601-2-80:2018 [Withdrawn]
Medical electrical equipment — Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
|
95.99 | |
|
ISO 80601-2-84:2020 [Withdrawn]
Medical electrical equipment — Part 2-84: Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment
|
95.99 | |
|
Medical electrical equipment — Part 2-85: Particular requirements for the basic safety and essential performance of cerebral tissue oximeter equipment
|
90.93 | |
|
Medical electrical equipment — Part 2-87: Particular requirements for basic safety and essential performance of high-frequency ventilators
|
90.20 | |
|
Medical electrical equipment — Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs — Amendment 1
|
60.60 | |
|
IEC 80601-2-30:2009/Amd 1:2013 [Withdrawn]
Medical electrical equipment — Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers — Amendment 1
|
95.99 | |
|
Medical electrical equipment — Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment — Amendment 1
|
60.60 | |
|
ISO 80601-2-12:2011/Cor 1:2011 [Withdrawn]
Medical electrical equipment — Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators — Technical Corrigendum 1
|
95.99 | |
|
Medical electrical equipment — Part 2-71: Particular requirements for the basic safety and essential performance of functional near-infrared spectroscopy (functional NIRS) equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients
|
60.60 | |
|
ISO 80601-2-74:2021 [Withdrawn]
Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
|
95.99 | |
|
Medical electrical equipment — Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
|
60.60 | |
|
Medical electrical equipment — Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
|
60.60 | |
|
Medical electrical equipment — Part 2-84: Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment
|
60.60 | |
|
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers
|
90.92 | |
|
Medical electrical equipment — Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening
|
90.93 | |
|
ISO 80601-2-12:2020 [Withdrawn]
Medical electrical equipment — Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
|
95.99 | |
|
Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
|
90.92 | |
|
ISO 80601-2-61:2017 [Withdrawn]
Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
|
95.99 | |
|
ISO 80601-2-67:2020 [Withdrawn]
Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment
|
95.99 | |
|
ISO 80601-2-69:2020 [Withdrawn]
Medical electrical equipment — Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment
|
95.99 | |
|
ISO 80601-2-70:2020 [Withdrawn]
Medical electrical equipment — Part 2-70: Particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment
|
95.99 | |
|
Medical electrical equipment — Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening — Amendment 1
|
60.60 | |
|
Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement — Amendment 1
|
60.60 | |
|
IEC/DIS 80601-2-30 [Under development]
Medical electrical equipment — Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers
|
40.60 | |
|
Medical electrical equipment — Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
|
60.60 | |
|
Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-69: Particular requirements for the basic safety and essential performance of oxygen concentrator equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment
|
60.60 | |
|
Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
|
60.60 | |
|
ISO/DIS 80601-2-56 [Under development]
Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
|
40.60 | |
|
Non-invasive sphygmomanometers — Part 1: Requirements and test methods for non-automated measurement type
|
90.93 | |
|
ISO 81060-2:2009 [Withdrawn]
Non-invasive sphygmomanometers — Part 2: Clinical validation of automated measurement type
|
95.99 | |
|
ISO 81060-2:2009/Cor 1:2011 [Withdrawn]
Non-invasive sphygmomanometers — Part 2: Clinical validation of automated measurement type — Technical Corrigendum 1
|
95.99 | |
|
ISO 81060-2:2013 [Withdrawn]
Non-invasive sphygmomanometers — Part 2: Clinical investigation of automated measurement type
|
95.99 | |
|
Non-invasive sphygmomanometers — Part 2: Clinical investigation of intermittent automated measurement type
|
90.92 | |
|
Non-invasive sphygmomanometers — Part 2: Clinical investigation of intermittent automated measurement type — Amendment 1
|
60.60 | |
|
Non-invasive sphygmomanometers — Part 2: Clinical investigation of intermittent automated measurement type — Amendment 2
|
60.60 | |
|
ISO/DIS 81060-2 [Under development]
Non-invasive sphygmomanometers — Part 2: Clinical performance verification of intermittent automated measurement type
|
40.00 | |
|
Non-invasive sphygmomanometers — Part 3: Clinical investigation of continuous automated measurement type
|
90.92 | |
|
ISO/AWI 81060-3 [Under development]
Non-invasive sphygmomanometers — Part 3: Clinical performance verification of continuous automated measurement type
|
10.99 |
|
|
Non-invasive sphygmomanometers — Part 5: Requirements for the repeatability and reproducibility of NIBP simulators for testing of automated non-invasive sphygmomanometers
|
90.20 | |
|
ISO/CD 81060-7 [Under development]
Non-invasive sphygmomanometers — Part 7: Clinical performance verification of intermittent or repeated intermittent cuffless measurement type
|
30.60 |
|
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