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["附件3"]
["广东省内有源医疗器械产品情况摸查表"]
["填报单位：                                                                                                                                                                                         填报日期："]
["序号","产品名称","管理类别","境内/进口","注册证号","注册证到期时间","注册人","进口器械境内代理人","备案编号","备案人","产品涉及的新版GB9706系列标准编号",null,null,"是否已送检","送检/计划送检时间","送检/计划送检检测机构","是否已申请变更注册","是否已申请延续注册","联系人","联系电话"]
[{"$nulls":10},"通标","并标","专标"]
{"$rows_empty":12}
["填表说明：\n1.本表用于摸查广东省内注册、备案、进口代理人涉及的已注册和在研的有源医疗器械产品信息，以及后续送检、申请变更及延续的时间安排。\n2.“管理类别”栏，请填写：一类、二类、三类、在研。\n3.“产品涉及的新版GB9706系列标准编号”栏，涉及2个以上标准的，请用“；”隔开。\n3.日期请以“XXXX年XX月XX日”格式填写。\n4.产品不涉及的栏打“/”。"]

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