NF EN 60601-2-30

NF EN 60601-2-30

August 2002
Standard Cancelled

Medical electrical equipment - Part 2-30 : particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment

Le présent document traite de la sécurité et spécifie les performances essentielles des appareils de surveillance de la pression sanguine prélevée de façon non invasive, automatiquement et périodiquement.

Main informations

Collections

National standards and national normative documents

Publication date

August 2002

Number of pages

51 p.

Reference

NF EN 60601-2-30

ICS Codes

11.040.55   Diagnostic equipment

Classification index

C74-388

Print number

1 - 23/08/2002

International kinship

IEC 60601-2-30:1999

European kinship

EN 60601-2-30:2000
Sumary
Medical electrical equipment - Part 2-30 : particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment

Le présent document traite de la sécurité et spécifie les performances essentielles des appareils de surveillance de la pression sanguine prélevée de façon non invasive, automatiquement et périodiquement.
Replaced standards (1)
NF EN 60601-2-30
January 1996
Standard Cancelled
Medical electrical equipment. Part 2 : particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment.

Ce document traite de la sécurité des appareils de surveillance de la pression sanguine prélevée indirectement, automatiquement et périodiquement.

Standard replaced by (1)
NF EN 80601-2-30
January 2011
Standard Cancelled
Medical electrical equipment - Part 2-30 : particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers

Le présent document s'applique à la sécurité de base et aux performances essentielles des sphygmomanomètres automatiques qui, au moyen d'un brassard gonflable, sont utilisés pour la mesure indirecte intermittente de la pression artérielle sans ponction artérielle. Il couvre les appareils em à énergie électrique de mesure indirecte intermittente de la pression artérielle sans ponction artérielle, comportant des méthodes automatiques pour l'estimation de la pression artérielle, y compris les moniteurs de pression artérielle pour l'environnement des soins à domicile. Le présent document entre dans le champ d'application de la Directive dispositifs médicaux 93/42/CEE.

ZOOM ON ... the Requirements department
To comply with a standard, you need to quickly understand its issues in order to determine its impact on your activity.

The Requirements department helps you quickly locate within the normative text:
- mandatory clauses to satisfy,
- non-essential but useful clauses to know, such as permissions and recommendations.

The identification of these types of clauses is based on the document “ISO / IEC Directives, Part 2 - Principles and rules of structure and drafting of ISO documents ”as well as on a constantly enriched list of verbal forms.

With Requirements, quickly access the main part of the normative text!

With Requirements, quickly access the main part of the normative text!
Need to identify, monitor and decipher standards?

COBAZ is the simple and effective solution to meet the normative needs related to your activity, in France and abroad.

Available by subscription, CObaz is THE modular solution to compose according to your needs today and tomorrow. Quickly discover CObaz!

Request your free, no-obligation live demo

I discover COBAZ