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EN 60601-2-10:2000/A1:2001 Standard

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  Keywords:

#stimulators #defibrillators #implanted #electrodes #brain

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulatorsIEC 60601-2-10:1987

  Purpose

Other names: IEC 60601-2-10:1987/A1:2001 Specifies particular requirements for the safety of electrical stimulators of muscles and nerves in the specialized practice of physical medicine. It excludes stimulators used with implanted electrodes, brain stimulation, neurological research, cardiac pacemakers, defibrillators and other surgical procedures.

  Publication

Friday 17th of November 2017

  Amendment

This standard is an amendment for "EN 60601-2-10:2000"

  Reference

This standard supersedes the "EN 60601-2-10:2000"

Anyway is still possible use the "EN 60601-2-10:2000" until November 1st, 2004

  Related Standards

EN 60601-2-10:2000

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulatorsIEC 60601-2-10:198...

EN ISO 5840:2009

Medical devices Directive (93/42/EEC)

Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005)

EN 60601-2-4:2011

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Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibri...

EN 45502-2-2:2008

Active implantable medical devices Directive (90/385/EEC)

Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat ta...

EN 45502-2-2:2008/AC:2009

Active implantable medical devices Directive (90/385/EEC)

Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat ta...

EN 45502-2-3:2010

Active implantable medical devices Directive (90/385/EEC)

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems

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