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EVS-EN IEC/IEEE 62209-1528:2021

Measurement procedure for the assessment of specific absorption rate of human exposure to radio frequency fields from hand-held and body-mounted wireless communication devices - Part 1528: Human models, instrumentation, and procedures (Frequency range of 4 MHz to 10 GHz)

General information
Valid from 01.12.2021
Base Documents
IEC/IEEE 62209-1528:2020; EN IEC/IEEE 62209-1528:2021
Directives or regulations
None
Standard history
Status
Date
Type
Name
16.07.2019
Amendment
06.12.2016
Main
06.09.2010
Main
This document specifies protocols and test procedures for the reproducible and repeatable measurement of the conservative exposure peak spatial average SAR (psSAR) induced inside a simplified model of the head and the body by radio-frequency (RF) transmitting devices, with a defined measurement uncertainty. These protocols and procedures apply to a significant majority of the population, including children, during the use of hand-held and body-worn wireless communication devices. These devices include single or multiple transmitters or antennas, and are operated with their radiating structure(s) at distances up to 200 mm from a human head or body. This document is employed to evaluate SAR compliance of different types of wireless communication devices used next to the ear, in front of the face, mounted on the body, operating in conjunction with other RF-transmitting, non-transmitting devices or accessories (e.g. belt-clips), or embedded in garments. The applicable frequency range is from 4 MHz to 10 GHz. Devices operating in the applicable frequency range can be tested using the phantoms and other requirements defined in this document. The device categories covered include, but are not limited to, mobile telephones, cordless microphones, and radio transmitters in personal, desktop and laptop computers, for multi-band operations using single or multiple antennas, including push-to-talk devices. This document can also be applied for wireless power transfer devices operating above 4 MHz. This document does not apply to implanted medical devices.
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