2
10
111100000000271742
北京市药品监督管理局
第二类医疗器械（不包含体外诊断试剂）产品说明书变更的审核
1111000000002717422111046007000
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市药监局
110000000000
北京市药品监督管理局
法定工作日: 上午08:30 - 12:00、下午12:00 - 17:30； 周六：上午：08:30 - 12:30（需预约）；法定节假日不对外服务。;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
第十六条 经食品药品监督管理部门注册审查的医疗器械说明书的内容不得擅自更改。已注册的医疗器械发生注册变更的，申请人应当在取得变更文件后，依据变更文件自行修改说明书和标签。说明书的其他内容发生变化的，应当向医疗器械注册的审批部门书面告知，并提交说明书更改情况对比说明等相关文件。审批部门自收到书面告知之日起20个工作日内未发出不予同意通知件的，说明书更改生效。（来源：医疗器械说明书和标签管理规定）1．申请材料应真实、完整、清晰、整洁，逐份加盖企业公章，要求签字的须签字。2．注册人填报的表格和编写的申请材料均应为A4规格纸张，政府及其他机构出具的文件按原件尺寸提供。 3．凡申请材料应提交复印件的，复印件应清晰，并应在复印件上注明日期，加盖企业公章。
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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%2Fxzsp.yjj.beijing.gov.cn%3A8088%2Fssologin%3FmatterCode%3D1111000000002717422111046007000
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第二类医疗器械（不包含体外诊断试剂）产品说明书变更的审核
北京市
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