UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

NEN - 93/42/EEG

Richtlijn 93/42/EEG van de Raad van 14 juni 1993 betreffende medische hulpmiddelen

active, Most Current
Organization: NEN
Publication Date: 12 July 1993
Status: active

Document History

93/42/EEG
July 12, 1993
Richtlijn 93/42/EEG van de Raad van 14 juni 1993 betreffende medische hulpmiddelen
A description is not available for this item.
93/42/EEG
July 12, 1993
Richtlijn 93/42/EEG van de Raad van 14 juni 1993 betreffende medische hulpmiddelen
A description is not available for this item.

References

This document is referenced by:
NEN 10601-1-2 - Medical electrical equipment - Part 1: General requirements for safety - Section 2: Collateral Standard - Electromagnetic compatibility - Requirements and tests
Published by NEN on August 1, 1993
This standard applies only to Medical Electrical Equipment, Medical Electrical Systems, Information Technology Equipment used in medical electrical application, and all other equipment forming part...
This document is referenced by:
NEN 10601-2-17 - Medical electrical equipment - Part 2-17: Particular requirements for the safety of remote-controlled automatically-driven gamma-ray after-loading equipment
Published by NEN on April 1, 1996
Establishes particular requirements for the safety of remote-controlled automatically-drive electromedical equipment for gamma-ray therapy of human subjects using afterloading. Its specifications...
This document is referenced by:
NEN 10601-2-18 - Medical electrical equipment - Part 2-18: Particular requirements for the safety of endoscopic equipment
Published by NEN on November 1, 1996
Specifies requirements for the safety of endoscopic equipment and its interconnection conditions with endoscopically-used accessories.
This document is referenced by:
NEN 10601-2-20 - Medical electrical equipment - Part 2-20: Particular requirements for the safety of transport incubators
Published by NEN on February 1, 1997
Establishes particular safety requirements and specifies tests to verify compliance with it. Does not apply to baby incubators or radiant warmers.
This document is referenced by:
NEN 10601-2-21/A1 - Medical electrical equipment - Part 2-21: Particular requirements for the safety of infant radiant warmers
Published by NEN on February 1, 1997
A description is not available for this item.
View Less
View All
Advertisement