02.
二类——市药监局办理医疗器械经营备案第二类医疗器械是具有中度风险，需要严格控制管理以保证其安全有效的医疗器械，比如我们日常生活中常见的创可贴、避孕套、体温计、血压计、制氧机、雾化器等，其产品和生产活动由省级食品药品监管部门实行许可管理，分别发给《医疗器械注册证》和《医疗器械生产许可证》。经营活动由设区的市级食品药品监管部门实行备案管理;
03.
三类——国家药监局办理医疗器械许可证第三类医疗器械是具有较高风险，需要采取特别措施严格控制管理以保证其安全有效的医疗器械，比如常见的输液器、注射器、静脉留置针、心脏支架、呼吸机、CT、核磁共振等，其产品和生产经营活动分别由、省级食品药品监管部门和设区的市食品药品监管部门实行许可管理，分别发给《医疗器械注册证》、《医疗器械生产许可证》、《医疗器械经营许可证》。
北京公司如何办理增加医疗器械经营范围呢?增加医疗器械经营范围有什么要求呢?徐冰为您详细介绍：
一、公司增加一类医疗器械经营范围
第一类医疗器械是指，通过常规管理足以保证其安全性、有效性的医疗器械。
一类医疗许可证无需办理经营许可证。如果是生产医疗器械，则需要到相关部门备案。
administration for medical device business for the secondtype of medical equipment is a moderate risk, need to strictlycontrol management to ensure its safe and effective medicaldevices, such as our daily life, band, condoms, thermometer, bloodmonitor, oxygen generator, atomizer, its products and productionactivities by the provincial food and drug regulatory departmentlicensing management, respectively issued to the medical deviceregistration certificate and medical device production license.Business activities shall be put on record by the food and drugregulatory departments of the city divided into districts; 03.Three —— state food and drug administration license the thirdcategory of medical devices is a high risk, take special measuresto strictly control and management to ensure its safe and effectivemedical devices, such as common infusion, syringe, intravenousneedle, heart stent, ventilator, CT, NMR, etc., its products andproduction and business activities by the state administration,provincial food and drug regulatory authorities and the municipalfood and drug regulatory departments licensing management,respectively issued to the medic
