朝阳南沙滩北京医疗器械三类经营许可证，医疗器械二类备案提供人员库房专业快捷包下证。

三类医疗器械经营许可证办理所需大致资料:

1、企业经营执照;2、企业负责人以及质检人员和技术人员的身份、学历、职称证明;3、经营场所证明以及地理位置图。

三类医疗器械经营许可证办理之后需要明确的几个注意事项

1、医疗器械经营许可证的有效期只有5年。有效期届满需要延续的，医疗器械经营企业应当在有效期届满6个月前，向原发证部门提出《医疗器械经营许可证》延续申请。

2、应当具有符合医疗器械经营质量管理要求的计算机信息管理系统，保证经营产品的可追溯。

3、应当建立销售记录制度和建立质量管理自查制度。

4、自行停业一年以上，重新经营时，应当提前书面报告所在地设区的市级食品药品监督管理部门，经核查符合要求后方可恢复经营。

关于在京办理三类医疗器械经营许可证的更多问题，欢迎私信小编，

upon expiration, the medical device trading enterprise shall, 6 months before the expiration of the validity period, apply to the original license issuing department for the renewal of the Medical Device Business License. 2. It shall have a computer information management system that meets the requirements of business quality management of medical devices to ensure the traceability of business products. 3. A sales record system and a quality management self-inspection system shall be established. 4. When suspending business for more than one year and re-operating, it shall submit a written report in advance to the food and drug supervisory and administrative department of the city where it is located, and shall resume business only after checking that it meets the requirements. For more questions about handling the third type of medical device business license in Beijing