CE_AlexMED_EMC
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Of Conformity EU Council Directive 2014/30/EU Electromagnetic Compatibility Registration No.: Product Identification Beijing LaserTell Medical Co., Ltd. Block1, No.12 Jingsheng South 2nd Rd., JQ Science Park, Tongzhou District, Beijing, China Beauty Devices Model No. : AlexMED, AlexMED Pro, DepiMED, DepiMED Pro, NdMED, ClearMED, FemiMED, VenaMED, EpiMED, EpiMED Pro, TruMED, ExtrMED, iMED, PluShape, PluShape Pro, HydroCoolol, Faceage, 4Deepoo : LaserTell Trade Mark Rating Test Standards EN 55014-1: 2017 EN 61000-3-2: 2014 EN 61000-3-3: 2013 EN 55014-2: 2015 The certificate of conformity is based on an evaluation of a sample of the above-mentioned product. Technical report and documentation are at the applicant’s disposal. This is to certify that the tested sample is in conformity with all provisions of Annex ll of Council Directive 2014/30/EU, in its latest amended version, referred to EMC Directive. The certificate does not imply assessment of the production and does not permit the use of Lab’s logo. The applicant of the certificate is authorized to use this certificate in connection with EU declaration of conformity to Article 15 of the Directive. Certified by Sally Zhang Manager The CE Marking may only be used if all relevant and effective EU Directives are complied with Shenzhen Anbotek Compliance Laboratory Limited 1/F, Building D, Sogood Science and Technology Park, Sanwei community, Hangcheng Street, Bao'an District, Shenzhen, Guangdong, China.518102 Tel: (86)755-26066440 Fax: (86)755-26014772 Email: service@anbotek.com Http://www.anbotek.co