Security vulnerabilities in healthcare are putting people at risk. While designing with wireless functionality has improved the transfer of information and expanded the benefits of medical devices, it requires additional security measures. Adopting Cybersecurity Guidelines for Wireless Medical Devices The U....
欧盟授权代表EC Representative 所在地 上海市崇明区长兴镇潘园公路2528号B幢21031室 联系电话 13818104617 手机 13818104617 销售总监 袁小姐 请说明来自顺企网,优惠更多 请卖家联系我 13818104617 详细介绍 我们的咨询业务 1:MDR法规培训 ,新法规立法过程、变化及转换期 ,MDR覆盖的范围,包括和MDD, AIMD的修订要点及...
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
MedNet EC-REP provides top-notch services as a European Authorized Representative (EC-REP), UK Responsible Person, and Swiss Authorized Representative. We specialize in medical devices, in vitro diagnostics, cosmetics, and personal protective equipment. Our team ensures fast and efficient market entry...
Procedure whereby the manufacturer or his authorized representative established in the European Community ensures and declares that the medical devices which have been subject to conformity examinations and tests (among other things, examination of every product or statistical control of products by random...
DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98...
Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific ...