{"s":true,"m":"没有数据！","d":{"id":3491,"keyword":"二类医疗器械注册证","classfyName":"医疗事故","status":1,"articleNum":32,"askNum":21,"contractNum":18,"classfyId":30,"deleted":false,"createTime":1574407466000,"pictureUrl":"/_/boss/3/onestopservice//20203/21/1587451264592/6aed31f57ca7445297a00787f4feaee5.png","url":"https://www.haolvshi.com.cn/flzs/3491.html","mUrl":"https://m.haolvshi.com.cn/flzs/3491.html","title":"二类医疗器械注册证_分类规则_法律责任-法律知识-好律师网","keywords":"二类医疗器械注册证，二类医疗器械分类规则","description":"二类医疗器械注册证：医疗器械注册，是指依照法定程序，对拟上市销售、使用的医疗器械的安全性、有效性进行系统评价，以决定是否同意其销售、使用的过程。它分为境内医疗器械注册和境外医疗器械注册，境外的医疗器械不管是一类，二类，三类都要到北京国家食品药品监督局办理：境内的一，二类医疗器械在当地的省或市食品药品监督局办理，三类的到国家食品药品监督局办理。医疗器械注册证是指医疗器械产品的合法身份证。","updateTime":1587451265000}}