{"s":true,"m":"没有数据！","d":{"id":3459,"keyword":"医疗器械三证","classfyName":"医疗事故","status":1,"articleNum":25,"askNum":16,"contractNum":11,"classfyId":30,"deleted":false,"createTime":1574407465000,"pictureUrl":"/_/boss/3/onestopservice//20202/27/1585289719210/27e0fe91dc04456b9acfdd2c476f0f7b.png","url":"https://www.haolvshi.com.cn/flzs/3459.html","mUrl":"https://m.haolvshi.com.cn/flzs/3459.html","title":"医疗器械三证-医疗器械分类规则-法律知识-好律师网","keywords":"医疗器械三证，医疗器械分类规则","description":"医疗器械三证：医疗器械是指直接或者间接用于人体的仪器、设备、器具、体外诊断试剂及校准物、材料以及其他类似或者相关的物品，包括所需要的计算机软件。“三证”：即医疗器械生产企业许可证、医疗器械经营许可证、准字号的医疗器械注册证。“一表”：医疗器械广告审查表。","updateTime":1585289950000}}