医疗器械产品分为一类、二类、三类;
一类:不用办理医疗器械许可证
第一类医疗器械是风险程度低、实行常规管理可以保证其安全有效的医疗器械，比如手术刀、手术剪、手动病床、医用冰袋、降温贴等，其产品和生产活动由所
在地设区的市级食品药品监管部门实行备案管理，经营活动则全部放开，既不用许可也不用备案，只需取得工商部门核发的营业执照即可。
二类:市药监局办理医疗器械经营备
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
1. What is a medical device? Beijing wants to understand the enterprises to see here Medical device: refers to instruments, equipment, appliances, materials or other articles used individually or in combination, including required software; their function on the surface of the body is not obtained by pharmacological, immunology or metabolic means, but may participate and play a certain auxiliary role. 2. How many categories are medical devices divided into? There are three categories: The operation of the first type of medical devices does
