3
10
11110000000057840H
北京市海淀区市场监督管理局
第一类医疗器械变更备案
11110000000057840H311104601400001
11110000000057840H3111046014000
0
889b689f-c6c6-402c-8fc4-25b1f81fb845
b5d95a76-6d8c-4257-8770-a92fc7b214c3
3
10
海淀区市场监管局
110108000000
北京市海淀区市场监督管理局
海淀区政务服务中心（上地办公区）：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; 中午12:00 - 13:30; 下午17:00 - 17:30; 周六上午08:30 - 12:30; )；
海淀区政务服务中心（上地办公区）：北京市海淀区东北旺南路甲29号二层西侧61-67号窗口；
第十五条 第一类医疗器械产品备案，由备案人向所在地设区的市级人民政府负责药品监督管理的部门提交备案资料。（来源：医疗器械监督管理条例）
（一）备案资料完整齐备。备案表填写完整。
（二）各项文件除关联文件外均应以中文形式提供。如关联文件为外文形式还应提供中文译本并由代理人签章。根据外文资料翻译的资料，应当同时提供原文。
（三）产品备案资料如无特殊说明的，应当由备案人签章。“签章”是指：备案人盖公章，或者其法定代表人、负责人签名加盖备案人公章。
（四）备案人提交纸质备案资料的，备案资料应当有所提交资料目录，包括备案资料的一级和二级标题，并以表格形式说明每项的页码。
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https://yzt.beijing.gov.cn/am/oauth2/authorize?service=bjzwService&response_type=code&client_id=000027174_04&scope=cn+uid+idCardNumber+reserve3+extProperties+credenceClass&redirect_uri=http%3A%2F%2F36.112.140.7%3A8088%2Fssologin%3FmatterCode%3D11110000000057840H311104601400001
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第一类医疗器械变更备案
北京市
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