大兴黄村北京医疗器械三类经营许可证，医疗器械二类备案提供进销存软件人员专业快捷包下证

类医疗器械备案要求，根据《医疗器械监督管理条例》凡是从事二类医疗器械经营的单位都需要到所在地设区的市级食品药品监督管理部门备案，二类医疗器械是具有中度风险，需要控制管理以保证其安全、有效的医疗器械。如：医用缝合针、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

注：二类医疗器械备案有效期为长期，到期前6个月到所在地设区的市级食品药品监督管理部门换发二类医疗器械备案新凭证

s and need to be controlled and managed to ensure their safe andeffective medical devices. Such as: medical suture needle,sphygmomanometer, thermometer, electrocardiogram machine,electroencephalography machine, microscope, acupuncture needle,biochemical analysis system, hearing aid, ultrasonic disinfectionequipment, non-absorbable sutures, etc. ask: 1. Commercial office60 square, storage 40 square 2.2 medical professionals are theleaders of the enterprise 3. Product management catalogue Note: Ifthe line of the above 3 points, basically can handle the record ofclass II medical devices Provide materials 1. Application form forfiling of Class II medical devices 2. Business license or pre-checkname notice 3. Copy of the identity certificate, educationbackground or professional title certificate of the legalrepresentative, the person in charge of the enterprise and theperson in charge of quality 4. Copy of the geographical locationmap, floor plan, house property right certificate or leaseagreement (attached with the house property right certificate). 56. Product qualification certificate 7. Last home purchase andsales contract and purchase channels Note: The validity period ofclass II medical devices is long-term, and the new recordcertificate of Class II medical devices shall be issued to themunicipal food and drug regulatory departme