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Normas BSI – AENOR
BS EN 50527-2-1:2016 - TC

BS EN 50527-2-1:2016 - TC

Tracked Changes. Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices. Specific assessment for workers with cardiac pacemakers

Fecha:
2020-02-25 /Definitive
Comité:
GEL/106
Resumen:
This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted pacemakers. It offers different approaches for doing the risk assessment. The most suitable one will be used. If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they need to be assessed separately. The purpose of the specific assessment is to determine the risk for workers with implanted pacemakers arising from exposure to electromagnetic fields at the workplace. The assessment includes the likelihood of clinically significant effects and takes account of both transient and long-term exposure within specific areas of the workplace. NOTE 1 This standard does not address risks from contact currents. The techniques described in the different approaches may also be used for the assessment of publicly accessible areas. The frequency range to be observed is from 0 Hz to 3 GHz. Above 3 GHz no interference with the pacemaker occurs when the exposure limits are not exceeded. NOTE 2 The rationale for limiting the observation range to 3 GHz can be found in ISO 14117:2012, Clause 5.
Keywords:
Electromagnetic compatibility, Magnetic fields, Physiological effects (human body), Hazards, Risk assessment, Implants (surgical), Human body, Electric fields, Electromagnetic radiation, Electromagnetic fields, Clinical testing, Frequencies, Environment (working), Measurement, Pacemakers, Electromagnetism, Occupational safety, Mathematical calculations, Electrical medical equipment
452,09
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