Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates当指令93/42/EEC第7.5节第2段附录I要求时,BS EN 15986:2011规定了医疗器械或医疗器械零件的标签要求,以表明存在邻苯二甲酸酯.这具体包括标签中使用的符号格式.BS EN 15986:2011未规定医疗...
35-EN_980-2008_Symbols_for_use_in_the_labelling_of_medical_devices 英文文献资料.pdf,EUROPEAN STANDARD EN 980 NORME EUROPÉENNE EUROPÄISCHE NORM May 2008 ICS 01.080.20; 11.120.01 Supersedes EN 980:2003 English version Symbols for use in the labelling
来自 hc-sc.gc.ca 喜欢 0 阅读量: 129 作者: Government of Canada, Health Canada, Health Products and Food Branch, Therapeutic Products Directorate, Medical Devices Bureau, Device Licensing Services Division 展开 摘要: 2004 Health Canada guidance document ...
EN ISO 15223-1:2012 Medical devices - Symbols to be used with medical device labels,Labelling and information to be supplied-Par 星级: 34 页 EN_980-2008_Symbols_for_use_in_the_labelling_of_medical_devices 星级: 37 页 EN_980-2008_Symbols_for_use_in_the_labelling_of_medical_devices...
Singapore has launched a voluntary scheme which rates medical devices according to their levels of cybersecurity provisions. The scheme aims to improve medical device security by incentivising manufacturers to adopt a security-by-design approach and enabling consumers and health care pro...
Batch management for products from the medical sector is regulated by the Medical Devices Act (MPG) of 1 January 1995. All companies that manufacture medical devices are obliged to label their products with a batch number (manufacturers, importers and retailers of medical devices). Under certain...
EN 980 - Symbols for use in the labelling of medical devices Published by CEN onMay 1, 2008 This European Standard specifies symbols for use in the information supplied by the manufacturer with medical devices. The requirements of this European Standard are not intended to apply to symbols......
Bob Tilling, VP global sales at Kallik draws on over two decades of industry experience to discuss the evolution of medical device trends, technology and regulation; and how digital platforms will be increasingly critical to navigate what lies ahead. 21 Oct 2021 Bob Tilling Medtech Regulatory Ins...
【英语版】国际标准 ISO 18113-1:2022 EN In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements 体外诊断医疗器械 制造商提供的信息(标签) 第1部分:术语、定义和一般要求.pdf 关闭预览 想预览更多内容,点击免费...
Operationally and reputationally, creators and suppliers of medical devices have much to gain by embracing e-labelling at their earliest opportunity. Benefits potentially span the whole business. They include: Open access to new markets; New process efficienci...