For years, I tried to escape, to fly away. This is my flag because I am Korean. The tu and this has been what I've been trying to run away from.Or maybe not exactly. More on that in a bit. For the past five years, I worked five different jobs, traveled to 10 countries, worked with four immigration lawyers, entered the visa lottery two times, and packed more suitcases than I can count.Almost nothing in my life lasted for more than a year. But there was one thing I stayed consistent about. My desire to work w ...

在俄罗斯及欧亚经济市场（EAEU）市场销售产品时，EAC符合性声明（Declaration of Conformity）是 重要的强制性认证文件。 一、确认产品是否需要EAC符合性声明 1. 适用范围 EAC声明适用于EAEU技术法规（TR CU/TR EAEU）清单中的产品（如低压设备、机械设备、玩具、 纺织品等）。部分高风险产品需EAC认证（CoC），而非声明（DoC）。 查询具体法规：参考TR CU/TR EAEU列表（如TR CU 004/2011（低压设备）、TR CU 020/2011（电磁 兼容性）等）。 2. 区分声明与认证 符合性声明（DoC）：由申请人自行准备文件，对产品符合性负责，通常用于中低风险产品。 符合性认证（CoC）：需由认证机构参与测试和审核，适用于高风险产品（如儿童用品、医疗器械 等）。 二、申请流程 # 1. 确定适用的技术法规和标准 明确产品对应的EAEU技术法规（如TR CU、TR EAEU）及协调标准（GOST、EN等）。 # 2. 准备技术文件 必需文件： 产品详细描述（技术护照、说明书、图纸等）； 原材料清单及供应商信息； 测试报告（需EAEU认可实验室出具，部分 ...

IRVINE, Calif., June 03, 2025 (GLOBE NEWSWIRE) -- ReShape Lifesciences® (Nasdaq: RSLS), the premier physician-led weight loss and metabolic health solutions company, today announced that its Quality Management System (QMS) and entire commercial portfolio of medical devices sold in Europe and in the United Kingdom (UK) have been certified under the European Union (EU) Medical Device Regulation (MDR) (EU) 2017/745 and UK Conformity Assessment (UKCA), respectively. The EU MDR, which replaced the Medical Device ...