口罩欧代MDD指令+注册+技术文档+符合性声明办理 深圳市MDD/MDR法规），全套CE技术文件编订， CE第四版临床评价（MEDDEV 2.7.1 Rev 4)编写，欧盟授权代表，欧盟自由销售证书，ISO13485:二016，(MDSAP)审核、美国FDA注册（含FDA510K申请），FDA美国代理人服务/ FDA QSR820验厂辅导及整改，FDA警告信应对&RED LIST 商，欧盟授权代表，进口商和分销商
直接供给的卫生机构或医疗保健专业人员(Article 25).
Store and keep the UDI for implantable devices by economic operators (Article 27.8)
Electronic system for registration of economic operators (Article 30+Annex VI, Part A)
Regulatory compliance
It should be ensured that supervision and control of the manufacture of devices, and the post-market surveillance and vigilance activities concerning them, are carried out within the manufacturer’s organisation by a person responsible for regulatory compliance who fulfils minimum conditions of qualification.
The authorised representative plays a pivotal role in ensuring the compliance of the devices produced by those manufacturers and in serving as their contact person established in the Union… legally liable for defective devices in the event that a manufacturer
established outside the Union has not complied with its general
obligations
