ČSN EN ISO 80601-2-67 (364801)

Zdravotnické elektrické přístroje - Část 2-67: Zvláštní požadavky na základní bezpečnost a nezbytnou funkčnost zařízení pro úsporu kyslíku (Norma k přímému použití jako ČSN).



NORMA vydaná dňa 1.5.2021


Jazyk
Prevedenie
DostupnosťSKLADOM
Cena23.60 bez DPH
23.60

Informácie o norme:

Označenie normy: ČSN EN ISO 80601-2-67
Rozlišovací znak: 364801
Katalógové číslo: 511895
Dátum vydania normy: 1.5.2021
Kód tovaru: NS-1023442
Počet strán: 72
Približná hmotnosť: 216 g (0.48 libier)
Krajina: Česká technická norma
Kategória: Technické normy ČSN

Anotácia textu normy ČSN EN ISO 80601-2-67 (364801):

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

Doporučujeme:




Cookies Cookies

Potrebujeme váš súhlas na využitie jednotlivých dát, aby sa vám okrem iného mohli ukazovať informácie týkajúce sa vašich záujmov. Súhlas udelíte kliknutím na tlačidlo „OK“.

Súhlas môžete odmietnuť tu.

Tu máte možnosť prispôsobiť si nastavenia súborov cookies v súlade s vlastnými preferenciami.

Potrebujeme váš súhlas na využitie jednotlivých dát, aby sa vám okrem iného mohli ukazovať informácie týkajúce sa vašich záujmov.