BS EN 50527-1 is a European standard on the procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices that discusses general risk assessment to ensure protection against radiation hazards.
BS EN 50527-1 is the first part of a multi-part series that provides a procedure to assess the risk to workers bearing one or more active implantable medical devices from exposure to electric, magnetic and electromagnetic fields at a workplace.
BS EN 50527-1 describes how a general risk assessment should be performed and determines whether it is necessary to carry out a detailed risk assessment.
Note1: BS EN 50527-1 does not cover indirect effects caused by non-active implants.
Note2: The risk of human exposure to EMF considered is only due to malfunctioning of AIMD. Possibilities of AIMD contribution to the risk, e.g., local modification of the distribution of EMF produced by external source or production of own EMF, are covered by the respective product standards for the AIMD.
Note3: Performance requirements concerning active implantable medical devices are excluded from the scope of BS EN 50527-1. These are defined in the relevant standards for active implantable medical devices.
BS EN 50527-1 on the assessment of the exposure to electromagnetic fields of workers is useful for:
An electromagnetic field (EMF) is an area of moving electrical charges. Some EMFs, especially those involving ionizing radiation, can be harmful. For most people, exposure to EMFs occurs daily, as the fields are virtually everywhere
BS EN 50527-1 provides you with risk assessment procedures, documentation, and information for the AIMD-Employee, maintaining the risk assessment, equipment with recommendations restricting the use, and much more.
The procedures provided by BS EN 50527-1 assist in the assessment of the exposure to electromagnetic fields of AIMD employees and ensure reduction against severe health issues due to EMF exposure.
With obedience and compliance to BS EN 50527-1, you can enhance the efficacy of the active implantable medical devices and enable protection to AIMD employees from EMF hazards.
BS EN 50527-1:2016 supersedes EN 50527-1:2010, which is withdrawn. BS EN 50527-1:2016 has made some technical changes compared to the previous edition EN 50527-1:2010. These include:
EN 50527-1:2016