International Organization for Standardization (ISO)
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ISO 17510-1:2007
Scope
IEC 60601-1:1988, Clause 1 applies, except as follows.
Amendment (add at the end of the Subclause 1.1):
This part of ISO 17510 specifies requirements for equipment intended for sleep apnoea breathing therapy for
domiciliary use, ships, aircraft and other transport vehicles and for use in healthcare institutions.
This part of ISO 17510 applies to equipment intended for use with adults and children, and excludes
equipment intended for use with neonates.
Jet and very high frequency ventilation and oscillation are not considered in this part of ISO 17510.
This part of ISO 17510 does not apply to equipment covered by the scope of the ISO 10651 series, including:
⎯ ISO 10651-2:2004;
⎯ ISO 10651-3:1997;
⎯ ISO 10651-4:2002;
⎯ ISO 10651-5:2006;
⎯ ISO 10651-6:2004.
This part of ISO 17510 does not apply to equipment covered by the scope of IEC 60601-2-12.
ISO 17510 covers sleep apnoea breathing therapy equipment for patient use. ISO 17510-2 applies to masks
and accessories used to connect sleep apnoea breathing therapy equipment to the patient. See also
Figure AA.1.
ISO 17510-1:2007 Referenced Document
IEC 60079-4 Electrical apparatus for explosive gas atmospheres - Part 4: Method of test for ignition temperature; Amendment 1
IEC 60529 Degrees of Protection Provided by Enclosures (IP Code) (Edition 2.1 ***Applies to French text only***)*, 2024-04-18 Update
IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety; Collateral standard: Safety requirements for medical electrical systems
IEC 60601-1-2:2007 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests
IEC 60601-1-6 Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability*, 2024-04-18 Update
IEC 60601-1-8:2006 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
IEC 60601-1:1988 Medical electrical equipment; part 1: general requirements for safety
ISO 14937 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices*, 2009-10-01 Update
ISO 14971:2007 Medical devices - Application of risk management to medical devices
ISO 15223-1:2007 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
ISO 17510-2:2007 Sleep apnoea breathing therapy - Part 2: Masks and application accessories
ISO 17664:2004 Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices
ISO 23328-1 Breathing system filters for anaesthetic and respiratory use - Part 1: Salt test method to assess filtration performance
ISO 23328-2 Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects
ISO 32 Gas cylinders for medical use; Marking for identification of content
ISO 3744:1994 Acoustics - Determination of sound power levels of noise sources using sound pressure - Engineering method in an essentially free field over a reflecting plane
ISO 4135:2001 Anaesthetic and respiratory equipment - Vocabulary
ISO 4871 Acoustics - Declaration and verification of noise emission values of machinery and equipment
ISO 5356-1 Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets*, 2015-03-01 Update
ISO 5356-2 Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors AMENDMENT 1*, 2012-01-01 Update
ISO 5359 Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases AMENDMENT 1*, 2014-01-01 Update
ISO 8185:2007 Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems
ISO 9170-1 Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum*, 2017-07-01 Update
ISO/TR 16142:2006 Medical devices - Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices