2
20
111100000000271742
北京市药品监督管理局
医疗器械产品出口销售证明
1111000000002717422112046006000
0
6f65581e-a9da-4362-ab9d-0fbf5aeb1543
f5fe77e1-34f2-429d-a2f6-5a4446a9663b
2
20
市药监局
110000000000
北京市药品监督管理局
北京市政务服务中心:法定工作日: 上午: 09:00 - 12:00; 下午: 13:30 - 17:00; (延时服务时间: 工作日上午08:30 - 09:00; 下午17:00 - 17:30; 周六上午09:00 - 13:00; );北京城市副中心政务服务中心:法定工作日: 上午: 09:00 - 12:00; 下午: 12:00 - 17:00; (延时服务时间: 工作日上午08:30 - 09:00; 下午17:00 - 17:30; 周六上午09:00 - 13:00; )
北京市政务服务中心:北京市丰台区西三环南路1号(六里桥西南角)综合窗口
北京城市副中心政务服务中心:北京市通州区新华东街48号二区（东南角）综合窗口
第二条 在我国已取得医疗器械产品注册证书及生产许可证书，或已办理医疗器械产品备案及生产备案的，食品药品监督管理部门可为相关生产企业（以下简称企业）出具《医疗器械产品出口销售证明》（来源：《国家食品药品监督管理总局关于发布医疗器械产品出口销售证明管理规定的通告》）。1．申请材料应当完整、清晰、签字并逐份加盖企业公章。使用A4纸打印或复印，装订成册；2．凡申请材料需提交复印件的，申请人须在复印件上注明日期，加盖企业公章；3．生产企业提交的《医疗器械产品出口销售证明登记表》应当有法定代表人签字并加盖企业公章；4．核对申请材料真实性的自我保证声明应当有法定代表人签字并加盖企业公章。
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