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ISO 80601-2-90:2021

Current

Current

The latest, up-to-date edition.

Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment

Available format(s)

Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users

Language(s)

French, English

Published date

30-08-2021

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 benefit from receiving high-flow humidified respiratory gases, which can include a patient whose upper airway is bypassed.

EXAMPLE1 Patients with Type 1 Respiratory Failure who exhibit a reduction in arterial blood oxygenation.

EXAMPLE2 Patients who would benefit from reduced work of breathing, as needed in Type 2 Respiratory Failure, where arterial carbon dioxide is high.

EXAMPLE3 Patients requiring humidification to improve mucociliary clearance.

Respiratory high-flow therapy equipment can be intended for use in the home healthcare environment or intended for use in professional healthcare facilities.

NOTE1 In the home healthcare environment, the supply mains is often not reliable.

Respiratory high-flow therapy equipment can be:

— fully integrated ME equipment; or

— a combination of separate items forming a ME system.

This standard also applies to other types of respiratory equipment when that equipment includes a respiratory high-flow therapy mode.

NOTE2 This standard and ISO80601-2-12[14] are applicable to a critical care ventilator with a high-flow therapy mode.

Respiratory high-flow therapy equipment can be transit-operable.

This document is also applicable to those accessories intended by their manufacturer to be connected to the respiratory high-flow therapy equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the respiratory high-flow therapy equipment.

EXAMPLE4 Breathing sets, connectors, humidifier, breathing system filter, external electrical power source, distributed alarm system, high-flow nasal cannula, tracheal tube, tracheostomy tube, face mask and supra-laryngeal airway.

If a clause or subclause is specifically intended to be applicable to MEequipment only, or to MEsystems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to MEequipment and to MEsystems, as relevant.

Hazards inherent in the intended physiological function of MEequipment or MEsystems within the scope of this document are not covered by specific requirements in this document except in the general standard, 7.2.13 and 8.4.1.

NOTE3 Additional information can be found in the general standard, 4.2.

This document does not specify the requirements for:

ventilators or accessories for ventilator-dependent patients intended for critical care applications, which are given in ISO80601‑2‑12[14];

ventilators or accessories intended for anaesthetic applications, which are given in ISO80601‑2‑13[15];

ventilators or accessories intended for the emergency medical services environment, which are given in ISO80601‑2‑84[20];

ventilators or accessories intended for ventilator-dependent patients in the home healthcare environment, which are given in ISO80601‑2‑72[17];

— ventilatory support equipment or accessories intended for patients with ventilatory impairment, which are given in ISO80601‑2‑79[18];

— ventilatory support equipment or accessories intended for patients with ventilatory insufficiency, which are given in ISO80601‑2‑80[19];

— sleep apnoea therapy MEequipment, which are given in ISO80601‑2‑70[16];

— continuous positive airway pressure (CPAP) MEequipment;

— high-frequency jet ventilators (HFJVs)[31], which are given in ISO80601‑2‑87[21];

— gas mixers for medical use, which are given in ISO11195[9];

— flowmeters, which are given in ISO15002[11];

— high-frequency oscillatory ventilators (HFOVs), which are given in ISO80601‑2‑87[21]; and

— cuirass or “iron-lung” ventilation equipment.

This document is a particular standard in the IEC60601 series, the IEC80601 series and the ISO80601 series.

Committee
ISO/TC 121/SC 3
DocumentType
Standard
Pages
100
PublisherName
International Organization for Standardization
Status
Current

I.S. EN ISO 80601-2-79:2024 Medical electrical equipment - Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment (ISO 80601-2-79:2024)

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