合针、血压计、体温计、心电图机、脑电图机、显微镜、针灸针、生化分析系统、助听器、超声消毒设备、不可吸收缝合线等。
要求：
1.商用性质办公60平，仓储40平
2.2名医学专业人员为企业负责人
3.产品经营目录
注：符合以上3点，基本上就可以办理二类医疗器械备案
提供材料
1.二类医疗器械备案申请书
2.营业执照或预先核名通知书
3.法定代表人、企业负责人、质量负责人的身份证明、学历或者职称证明复印件
4.经营场所、库房地址的地理位置图、平面图、房屋产权证明文件或者租赁协议(附房屋产权证明文件)复印件 5.产品经营目录表
6.产品合格证书
7.上家购销合同、进货渠道
ter, electrocardiogram machine, EEG machine, microscope, acupuncture needle, biochemical analysis system, hearing aid, ultrasonic disinfection e, non-absorbable sutures, etc. ask: 1. Commercial nature of the office 60 square, storage 40 square 2.2 medical professionals are the leaders of the enterprise 3. Product management catalogue Note: If the line of the above 3 points, basically can handle the record of class II medical devices Provide materials 1. Application for filing of Class II medical devices 2. Business license or pre-check name notice 3. Copy of the identity certificate, education background or professional title certificate of the legal representative, the person in charge of th
