Medical suction equipment — Part 4: General requirements
This document specifies general requirements for medical suction equipment that are common to all parts of the ISO 10079 series.
This document is not applicable to the following:
a) end-pieces such as suction catheters, drains, curettes, Yankauer suckers and suction tips;
b) syringes;
c) dental suction equipment;
d) anaesthetic gas scavenging systems;
e) laboratory suction;
f) autotransfusion…
Appareils électromédicaux — Partie 2-90: Exigences particulières pour la sécurité de base et les per...
Le présent document s'applique à la sécurité de base et aux performances essentielles des équipements de thérapie respiratoire à haut débit, tels que définis en 201.3.220, ci-après également désignés par appareils EM ou systèmes EM, en association avec leurs accessoires:
— destinés à être utilisés sur des patients qui peuvent respirer spontanément; et
— destinés à être utilisés chez des…
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
— intended for use with patients who can breathe spontaneously; and
— intended for patients who would benefit from improved alveolar gas exchange; and who would…
Medical electrical equipment - Part 2-90: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
- intended for use with patients who can breathe spontaneously; and
- intended for patients who would benefit from improved alveolar gas exchange; and who would…
Appareils électromédicaux - Partie 2-90: Exigences particulières pour la sécurité de base et les per...
Le présent document s'applique à la sécurité de base et aux performances essentielles des équipements de thérapie respiratoire à haut débit, tels que définis en 201.3.220, ci-après également désignés par appareils EM ou systèmes EM, en association avec leurs accessoires:
- destinés à être utilisés sur des patients qui peuvent respirer spontanément; et
- destinés à être utilisés chez des…
Multimedia systems and equipment - Multimedia e-publishing and e-books - Interchange format for e-di...
IEC 62605:2021 specifies the interchange format for e-dictionaries among publishers, content creators and manufacturers.
This document does not address the following aspects:
• data formats for reading devices;
• elements necessary for final print reproduction only;
• rendering issues related to physical devices;
• security issues such as DRM for documents.
IEC 62605:2021 cancels and…
Electrostatics - Part 5-4: Protection of electronic devices from electrostatic phenomena - Complianc...
IEC TS 61340-5-4:2021(E) describes compliance verification testing for technical items that are included in ESD control programs, such as those specified in IEC 61340-5-1.
Test methods are based on those specified in IEC 61340-5-1 and other parts of the IEC 61340 series, and are simplified where necessary for the purposes of compliance verification, to be performed by competent personnel.
Users…
Nuclear power plants - Instrumentation and control systems important to safety - Criteria for seismi...
IEC 63186:2021 specifies the minimum requirements for the design of the seismic trip system, and the components thereof, used in a nuclear power plant to mitigate seismic effects. This system is intended to shut down the reactor in operation automatically before it is significantly impacted by the vibratory ground motion incurred by strong earthquakes. This document is applicable to both the…
