I.S. EN 50527-2-2:2018
Current
The latest, up-to-date edition.
PROCEDURE FOR THE ASSESSMENT OF THE EXPOSURE TO ELECTROMAGNETIC FIELDS OF WORKERS BEARING ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-2: SPECIFIC ASSESSMENT FOR WORKERS WITH CARDIOVERTER DEFIBRILLATORS (ICDS)
Hardcopy , PDF
English
06-17-2018
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
National Foreword
European foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Specific assessment
5 Documentation
Annex A (normative) - Device specific replacement of
EN 50527-1:2016, Table 1
Annex B (informative) - Clinical investigation methods
Annex C (informative) - in vitro testing/measurements
Annex D (informative) - Modelling - Field modelling or
calculations
Annex E (informative) - Interference from Low-Frequency
Magnetic and Electric Fields (1 Hz to 10 MHz)
Including Application to 50 Hz Power-Frequency
Annex F (informative) - Determination of minimum immunity
for radio-frequency fields
Annex G (informative) - Obtaining the device immunity
and guidelines provided by device manufacturers
Bibliography
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