NF EN 60601-2-37/A1

September 2005

Standard Cancelled

Medical electrical equipment - Part 2-37 : particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

Le présent document constitue une modification technique de nombreux points de la norme NF EN 60601-2-37. Il précise les classifications CEM et les essais associés. Il comprend des méthodologies de mesurages normalisées.Ce document entre dans le champ d'application de la Directive "Dispositifs médicaux" n°93/42/CE du 14/06/1993 modifiée par 98/79/CE du 27/10/1998 par 2000/70/CE du 16/11/2000 et par 2001/104/CE du 7/12/2001.

View the extract

Main informations

Collections

National standards and national normative documents

Publication date

September 2005

Number of pages

19 p.

Reference

NF EN 60601-2-37/A1

ICS Codes

11.040.55 Diagnostic equipment

Classification index

C74-335/A1

Print number

1 - 03/10/2005

International kinship

IEC 60601-2-37/A1:2004

European kinship

EN 60601-2-37/A1:2005

Sumary

Medical electrical equipment - Part 2-37 : particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment

Le présent document constitue une modification technique de nombreux points de la norme NF EN 60601-2-37. Il précise les classifications CEM et les essais associés. Il comprend des méthodologies de mesurages normalisées. Ce document entre dans le champ d'application de la Directive "Dispositifs médicaux" n°93/42/CE du 14/06/1993 modifiée par 98/79/CE du 27/10/1998 par 2000/70/CE du 16/11/2000 et par 2001/104/CE du 7/12/2001.

Standard replaced by (1)

NF EN 60601-2-37

April 2008

Standard Current

Medical electrical equipment - Part 2-37 : particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment

Le présent document s'applique à la SECURITE DE BASE et aux PERFORMANCES ESSENTIELLES des APPAREILS DE DIAGNOSTIC A ULTRASONS comme définis en 201.3.217, désignés ci-après sous le terme APPAREILS EM. Ce document entre dans le champ d'application de la Directive n° 93/42/CEE du 14/06/1993 relative aux dispositifs médicaux.

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