Need help?

EN 60601-2-33:2010/A2:2015 Standard

wave
Save  

  Keywords:

#equipment #performance #safety #essential #medical

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosisIEC 60601IEC 60601-2-33:2010

  Purpose

Other names: IEC 60601-2-33:2010/A2:2015 Amendment to EN 60601-2-33:2010.

  Publication

Friday 17th of November 2017

  Amendment

This standard is an amendment for "EN 60601-2-33:2010"

  Reference

This standard supersedes the "EN 60601-2-33:2010/A1:2015 (IEC 60601-2-33:2010/A1:2013)"

Anyway is still possible use the "EN 60601-2-33:2010/A1:2015 (IEC 60601-2-33:2010/A1:2013)" until July 23rd, 2018

  Related Standards

EN ISO 21536:2009

Medical devices Directive (93/42/EEC)

Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2...

EN ISO 10993-7:2008/AC:2009

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)

EN ISO 10993-1:2009/AC:2010

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)

EN ISO 10993-3:2014

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:...

EN ISO 10993-4:2009

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd...

EN ISO 10993-5:2009

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)

  Stay up to date

CELAB is Notified Body No.2037 for the EMC Directive and Italian office of a Notified Body for the RED Directive.

CELAB performs voluntary inspection activities on technical construction files to check their contents.

CELAB can accomplish all the required tests in order to affix the CE-marking related to EMC, LVD, RED, MDD, machines and many others.

CLICK HERE TO GET TESTS AND INFO ON THE EN 60601-2-33:2010/A2:2015 STANDARD

  ACCESS

Search for a standard
GO

Register

Already a member?
Login

  OTHER APPLICATIONS

If you are interested in DO160 tests, you can give a try to our other free of charge software:
CE-Marking assistant, Version: 1.3.0