CleverPoint’ Product is intended to be used for research applications and personal use only. Our products are not sold as Medical Devices as defined in EU directive 93/42/EEC. Our products are not designed or intended to be used for diagnosis or treatment of disease.
Directives
2014/53/EU (RED)
2015/863/EU (RoHS)
Safety – RED, art. 3.1. a)
PN-EN IEC 62368-1 2020
EMC – RED, art. 3.1. a)
PN-EN 55032:2015-09
PN-EN 55035:2017-09/A11:2020-09
ETSI EN 301 489-1 V2.2.3 (2019-11)
ETSI EN 301 489-17 V3.2.4 (2020-09)
Radio – RED, art. 3.2
ETSI EN 300 328 V2.2.2 (2019-07)
RoHS
PN-EN IEC 63000:2019-01
Declaration of Conformity
Hereby, CleverPoint Sp. z o.o. declares that the radio equipment CleverPoint 4 complies with the requirements of the European Parliament and Council Directive 2014/53/EU of 16 April 2014 on the harmonization of the laws of the Member States relating to the making available on the market of radio equipment and repealing Directive 1999/5/EC.