Registration number (WIID)Project No.TitleStatus
62210LVS EN 50401:2018Product standard to demonstrate the compliance of base station equipment with radiofrequency electromagnetic field exposure limits (110 MHz - 100 GHz), when put into serviceStandarts spēkā
66708LVS EN 50527-2-3:2022Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-3: Specific assessment for workers with implantable neurostimulatorsStandarts spēkā
59047LV SEN 50527-2-1:2017Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 2-1: Specific assessment for workers with cardiac pacemakersStandarts spēkā
70529LVS CLC/TR 50713:2021Reasonably Foreseeable Use Conditions when referring to EMF Exposure AssessmentStandarts spēkā
59938LVS EN 62110:2010/AC:2015Electric and magnetic field levels generated by AC power systems - Measurement procedures with regard to public exposureStandarts spēkā
70792LVS EN IEC/IEEE 63195-2:2023Assessment of power density of human exposure to radio frequency fields from wireless devices in close proximity to the head and body (frequency range of 6 GHz to 300 GHz) - Part 2: Computational procedureStandarts spēkā
67142LVS EN 50554:2021Basic standard for the in-situ assessment of exposure to radio frequency electromagnetic fields in the vicinity of a broadcast siteStandarts spēkā
62811LVS CLC/TR 50442:2018Guidelines for product committees on the preparation of standards related to human exposure from electromagnetic fieldsStandarts spēkā
69850LVS EN 50360:2018/A1:2023Product standard to demonstrate the compliance of wireless communication devices, with the basic restrictions and exposure limit values related to human exposure to electromagnetic fields in the frequency range from 300 MHz to 6 GHz: devices used next to the earStandarts spēkā
59046LVS EN 50527-1:2017Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices - Part 1: GeneralStandarts spēkā
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