Detailní informace o produktu

Typ produktu Česká technická norma (ČSN)
Oznaèení zákl. dokumentu ČSN EN ISO 80601-2-67
Zmìna/oprava/svazek
Tøídicí znak 364801
Katalogové èíslo 511895
Název dokumentu Zdravotnické elektrické přístroje - Část 2-67: Zvláštní požadavky na základní bezpečnost a nezbytnou funkčnost zařízení pro úsporu kyslíku
Anglický název Medical electrical equipment - Part 2-67: Particular requirements for basic safety and essential performance of oxygen-conserving equipment
Datum vydání 01.05.2021
Datum ukonèení platnosti
Datum úèinnosti 01.06.2021
Vìstník vydání (mìs/rok) 5/21
Vìstník zrušení
Zpùsob vydání ve věstníku
Zpùsob pøevzetí originálu vyhlášením
Bude pøeložena Ne
Použité jazyky
ICS kódy 11.040.10 - Anesteziologická, respirační a resuscitační zařízení
Subsektor
Deskriptory
Klíèová slova
Harmonizace/Urèení Informace o harmonizovaných a urèených normách jsou zveøejnìny v Databázi harmonizovaných norem
Zapracované dokumenty
OznaèeníRok vydání
EN ISO 80601-2-672020
ISO 80601-2-672020
Zmìny
Opravy
Nahrazuje dokumenty
Katalogové èísloOznaèeníRok vydání
73721ČSN EN ISO 18779 2005
Byla nahrazena dokumenty
Anotace

ČSN EN ISO 80601-2-67 IEC 60601-1:2005+AMD1:2012, 1.1 is replaced by: This document is applicable to the basic safety and essential performance of oxygen conserving equipment, hereafter referred to as ME equipment, in combination with its accessories intended to conserve supplemental oxygen by delivering gas intermittently and synchronized with the patient's inspiratory cycle, when used in the home healthcare environment. Oxygen conserving equipment is typically used by a lay operator. NOTE 1 - Conserving equipment can also be used in professional health care facilities. This document is also applicable to conserving equipment that is incorporated with other equipment. EXAMPLE Conserving equipment combined with a pressure regulator[2], an oxygen concentrator[7] or liquid oxygen equipment[4]. This document is also applicable to those accessories intended by their manufacturer to be connected to conserving equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the conserving equipment. This document is intended to clarify the difference in operation of various conserving equipment models, as well as between the operation of conserving equipment and continuous flow oxygen equipment, by requiring standardized performance testing and labelling. This document is only applicable to active devices (e.g. pneumatically or electrically powered) and is not applicable to non-active devices (e.g. reservoir cannulas). 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 2 - Additional information can be found in IEC 60601-1:2005+AMD1:2012, 4.2.