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ILNAS-EN ISO 80601-2-12:2011 Edition 04/2011
Medizinische elektrische Geräte - Teil 2-12: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Beatmungsgeräten für die Intensivpflege (ISO 80601-2-12:2011)
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Abstract

ISO 80601-2-12:2011 applies to the basic safety and essential performance of a ventilator in combination with its accessories, hereafter referred to as me equipment: intended to be attended by a professional operator for those patients who are dependent on mechanical ventilation; and intended for use in critical care environments in a professional healthcare facility or intended for use in transport within a professional healthcare facility. ISO 80601-2-12:2011 is also applicable to those accessories intended by their manufacturer to be connected to a breathing system, or to a ventilator, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilator. ISO 80601-2-12:2011 is not applicable to me equipment or an me system operating in ventilation modes intended for patients who are not dependent on mechanical ventilation. ISO 80601-2-12:2011 is not applicable to me equipment or an me system intended for those patients who are not dependent on mechanical ventilation. 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. ISO 80601-2-12:2011 is not applicable to continuous positive airway pressure (CPAP) me equipment, sleep apnoea therapy me equipment, home healthcare environment ventilators, ventilatory support me equipment, emergency and transport ventilators, anaesthetic ventilators, high-frequency jet ventilators (HFJVs) and high-frequency oscillatory ventilators (HFOVs). ISO 80601-2-12:2011 does not specify the requirements for me equipment that is intended solely to augment the ventilation of spontaneously breathing patients within a professional healthcare facility. ISO 80601-2-12:2011 does not specify the requirements for ventilators or accessories intended for anaesthetic applications which are given in ISO 80601-2-13. ISO 80601-2-12:2011 does not specify the requirements for ventilators or accessories intended for home care ventilators for ventilator-dependent patients which are given in ISO 10651-2. ISO 80601-2-12:2011 does not specify the requirements for ventilators or accessories intended for emergency and transport which are given in ISO 10651-3. ISO 80601-2-12:2011 does not specify the requirements for ventilators or accessories intended for home-care ventilatory support devices which are given in ISO 10651-6.

Status

Standard - Zurückgezogen

Ursprung

Technisches Komitee :
CEN/TC 215 : Beatmungs- und Anästhesiegeräte

Richtlinien

93/42/EEC : Medical devices

Annahme

Beginn der Abstimmung über den Entwurf    23/07/2009   Datum der Ratifizierung (dor)    05/02/2011
Ende der Abstimmung über den Entwurf    23/12/2009   Datum der Ankündigung (doa)    31/07/2011
Beginn der Abstimmung über den Schlussentwurf    04/11/2010   Datum der Veröffentlichung (dop)    31/10/2011
Ende der Abstimmung über den Schlussentwurf    04/01/2011   Datum der Zurückziehung (dow)    15/04/2014


Veröffentlichung im Amtsblatt
des Grossherzogtum Luxemburg
05/01/2012
Referenz Mémorial A N° 2

Relations

Evolutions
ILNAS-EN ISO 80601-2-12:2020
ILNAS-EN ISO 80601-2-12:2011/AC:2011

Relations to older standards
ILNAS-EN 794-1:1997+A2:2009

Entspricht der/den internationalen Norm(en)
ISO 80601-2-12 
ISO 80601-2-12 
IEC/CD 80601-2-12 
ISO 80601-2-12:2011 
ISO 80601-2-12:2011 

Internationale Normungsklassifizierung (ICS) :

11.040.10 : Anaesthetic, respiratory and reanimation equipment

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