Standard Svensk standard · SS-EN ISO 80601-2-90:2021

Elektrisk utrustning för medicinskt bruk – Del 2-90: Särskilda krav på grundläggande säkerhet och väsentliga prestanda för respiratorisk utrustning för högflödesbehandling (ISO 80601-2-90:2021)

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Standard Svensk standard · SS-EN ISO 80601-2-90:2021

Elektrisk utrustning för medicinskt bruk – Del 2-90: Särskilda krav på grundläggande säkerhet och väsentliga prestanda för respiratorisk utrustning för högflödesbehandling (ISO 80601-2-90:2021)
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Omfattning
This document applies to the basic safety and essential performance of ventilatory high-flow therapy equipment, as defined in 201.3.204, hereafter also referred to as ME equipment, in combination with its accessories:
- intended for use in the home healthcare environment;
- intended for use in professional healthcare facilities;
- intended for use by a lay operator or a healthcare professional operator;
- intended for use with patients who can breathe spontaneously;
- intended for patients who would benefit from improved alveolar gas exchange; and who would benefit from receiving high-flow humidified respiratory gases, including a patient whose upper airway is bypassed; and
EXAMPLE 1 Patients with Type 1 Respiratory Failure, which exhibits a reduction in arterial blood oxygenation or patients who would benefit from reduced work of breathing, as needed in Type 2 Respiratory Failure, where arterial carbon dioxide is high.
- not intended for patients who are dependent on artificial ventilation for their life support.
NOTE 1 In the home healthcare environment, the supply mains is often not reliable.
Ventilatory high-flow therapy equipment is typically composed of four parts:
1) gas sources,
- air, and
- if needed, oxygen;
NOTE 2 Gas sources include medical gas pipeline systems, gas cylinders, oxygen concentrators and ambient air.
2) humidifier;
NOTE 3 When dry gas is utilized, a humidifier is typically needed.
3) breathing tube;
4) a patient interface, which is used to deliver gas to the patient; and
5) a flow controller, which is used to select and deliver the desired flow.
NOTE 4 The flow controller can be at a fixed rate.
NOTE 5 The flowrate range is dependent upon the intended patient population (e.g., neonatal, paediatric and adult patients can require different flowrates).
These parts can be combined (e.g., the gas source and humidifier can be combined). Ventilatory highflow therapy equipment interfaces with the patient whose upper airway is intact via a ...

Ämnesområden

Utrustning för anestesi, respiration och återupplivning (11.040.10)


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Standard Svensk standard · SS-EN ISO 80601-2-90:2021

Elektrisk utrustning för medicinskt bruk – Del 2-90: Särskilda krav på grundläggande säkerhet och väsentliga prestanda för respiratorisk utrustning för högflödesbehandling (ISO 80601-2-90:2021)
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Produktinformation

Språk: Engelska

Framtagen av: Anestesi- och respiratorutrustning, SIS/TK 329

Internationell titel: Medical electrical equipment - Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment (ISO 80601-2-90:2021)

Artikelnummer: STD-80031674

Utgåva: 1

Fastställd: 2021-10-12

Antal sidor: 108