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EVS-EN 303 520 V1.2.1:2019

Short Range Devices (SRD); Ultra Low Power (ULP) wireless medical capsule endoscopy devices operating in the band 430 MHz to 440 MHz; Harmonised Standard for access to radio spectrum

General information
Valid from 15.10.2019
Base Documents
ETSI EN 303 520 V1.2.1
Directives or regulations
2014/53/EU Radio equipment (RED)
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Directive 2014/53/EU (Radio equipment) notices: Notice 1: Compliance with this harmonised standard does not confer a presumption of conformity with the essential requirement set out in Article 3(2) of Directive 2014/53/EU if any of the following are applied: (a) with respect to clause B.1 of Annex B: ‘The manufacturer and test laboratory may agree on alternative suitable implementation of human torso simulator, which shall be then fully described in the test report’; (b) with respect to clause C.1 of Annex C: ‘Alternatively, the manufacturer and test laboratory may agree to use a Semi-Anechoic Room, the setup of which shall be then fully described in the test report’. Notice 2: The temperature referred to in clause B.2 of Annex B shall reflect the intended use.

Standard history

Status
Date
Type
Name
15.10.2019
Main
The present document specifies technical characteristics and methods of measurements for Ultra Low Power Wireless Medical Capsule Endoscopy application (CCam transmitters and associated DR receivers) operating in the designated frequency band 430 MHz to 440 MHz, as meant by ETSI TR 103 451.
A possible return (downlink) RF transmission channel from DR to CCam for command and control signalling, if and when implemented, is outside the scope of the present document.
NOTE: The relationship between the present document and essential requirements of article 3.2 of Directive 2014/53/EU is given in Annex A.
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Standard monitoring