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EN 60601-1-3:2008/A11:2016 Standard

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  Keywords:

#amendment #radiation #performance #collateral #standard

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipmentIEC 60601-1-3:2008

  Purpose

Amendment for EN 60601-1-3:2008.

  Publication

Friday 17th of November 2017

  Amendment

This standard is an amendment for "EN 60601-1-3:2008"

  Reference

This standard supersedes the "EN 60601-1-3:2008/AC:2010"

Anyway is still possible use the "EN 60601-1-3:2008/AC:2010" until November 1st, 2019

  Related Standards

EN ISO 5360:2009

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EN ISO 14937:2009

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Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, vali...

EN ISO 17664:2004

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Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical dev...

EN ISO 16201:2006

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Technical aids for disabled persons - Environmental control systems for daily living (ISO 16201:2006)

EN ISO 16061:2009

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Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2008, Corrected version...

EN 15986:2011

Medical devices Directive (93/42/EEC)

Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates

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