二、办理医疗器械三类经营许可证的流程是什么?
1. 提交申请
2. 窗口受理
3. 审核材料
4. 老师下户现场检查
5. 审批通过
6. 领取医疗器械三许可证
一、什么是医疗器械?
医疗器械:是指单独或者组合使用于人体的仪器、设备、器具、材料或者其他物品,包括所需要的软件;其用于人体体表及体内的作用不是用药理学、免疫学或者代谢的手段获得,可能有这些手段参与并起一定的辅助作用。
二、医疗器械分几类?
一共三类:
经营第一类医疗器械不需许可和备案,执照上面加上销售医疗器械一类就可以正常销售;
经营第二类医疗器械需要办理备案;
经营第三类医疗器械需要办理经营许可证。
三、办公室和库房需要多大面积?
根据Zui新法规要求:
6840体外诊断试剂含冷链:办公室30平,库房40平,冷链20立方米
剩下所有产品都是:办公室30平,库房40平
ogy or metabolic means, but may participate and play a certainauxiliary role. 2. How many categories are medical devices dividedinto? There are three categories: The operation of the first typeof medical devices does not need permission and record, the licenseplus the sales of medical devices can be sold normally; Theoperation of type II medical devices needs to be put on record; Theoperation of the third type of medical equipment requires theoperation license. How much area does the office and the warehouseneed? According to the latest regulatory requirements: 6840 Invitro diagnostic reagent includes cold chain: 30 square