Hivatkozási szám

MSZ EN ISO 80601-2-80:2020

Dokumentumazonosító

174250

Cím

Gyógyászati villamos készülékek. 2-80. rész: Légzési elégtelenség esetén használt légzéstámogató berendezések alapvető biztonságra és lényeges működésre vonatkozó kiegészítő követelményei (ISO 80601-2-80:2018)

Angol cím

Medical electrical equipment. Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency (ISO 80601-2-80:2018)

Alkalmazási terület

Replacement: This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of VENTILATORY SUPPORT EQUIPMENT, as defined in 201.3.205, for VENTILATORY INSUFFICIENCY, 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 by a LAY OPERATOR; — intended for use with PATIENTS who have VENTILATORY INSUFFICIENCY or failure, the most fragile of which would likely experience injury with the loss of this artificial ventilation; — intended for TRANSIT-OPERABLE use; — not intended for PATIENTS who are dependent on artificial ventilation for their immediate life support. EXAMPLE 1 PATIENTS with moderate to severe chronic obstructive pulmonary disease (COPD), moderate amyotrophic lateral sclerosis (ALS), severe bronchopulmonary dysplasia or muscular dystrophy. NOTE 1 In the HOME HEALTHCARE ENVIRONMENT, the SUPPLY MAINS is often not reliable. NOTE 2 Such VENTILATORY SUPPORT EQUIPMENT can also be used in non-critical care applications of professional health care facilities. This document is also applicable to those ACCESSORIES intended by their MANUFACTURER to be connected to the VENTILATOR BREATHING SYSTEM of VENTILATORY SUPPORT EQUIPMENT for VENTILATORY INSUFFICIENCY, where the characteristics of those ACCESSORIES can affect the BASIC SAFETY or ESSENTIAL PERFORMANCE of the VENTILATORY SUPPORT EQUIPMENT for VENTILATORY INSUFFICIENCY. EXAMPLE 2 Breathing sets, connectors, water traps, expiratory valve, HUMIDIFIER, BREATHING SYSTEM FILTER, external electrical power source, DISTRIBUTED ALARM SYSTEM. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS 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 ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+AMD1:2012, 7.2.13 and 8.4.1. NOTE 3 Additional information can be found in IEC 60601-1:2005+AMD1:2012, 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 ISO 80601-2-12; — VENTILATORS or ACCESSORIES intended for anaesthetic applications, which are given in ISO 80601-2-13[5]; — VENTILATORS or ACCESSORIES intended for the emergency medical services environment, which are given in ISO 80601-2-84[6]4, the future replacement for ISO 10651-3[7]; Túl hosszú scope

ICS

11.040.10 Altató-, érzéstelenítő-, lélegeztető- és újraélesztőberendezések

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2020-03-01

Forrás

idt ISO 80601-2-80:2018; idt EN ISO 80601-2-80:2019

Előd

MSZ EN ISO 10651-6:2009

Utód

Módosítás

Kiegészítő információk

SZK-közlemények

Kapcsolódó európai jogszabály

A szabvány

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