This document provides external medical device manufactures and end-users with guidance on how to evaluate their devices for interaction with radio frequency identification (RFID) systems. The test procedures in this document are based on experimental results from several AIM members to identify the RFID reader (operating under U.S. FCC guidelines) conditions that present the largest radio frequency (RF) spectrum. Test protocols are included for the major commercial implementations of RFID as standardized by ISO, including LF, HF, and UHF RFID. Both active and passive ISO RFID standards are covered in this document.
Published on 08.22.2016