医疗器械经营许可证办理依据《北京市实施细则（2017年修订版）》，具体提交材料如下：
1．《 医疗器械经营许可申请表》（原件1份）
2．《营业执照》复印件（交验原件）；（复印件1份）
3．法定代表人、企业负责人、质量负责人的身份证明（查验原件）、学历或者职称证明复印件（对于统一采购渠道，采取连锁经营的非法人零售企业，提供连锁企业总部质量负责人身份证明、学历或者职称证明复印件）；（交验原件）（复印件共3份）
4．企业基本情况（原件1份）。（内容包含：组织机构与部门设置说明、经营场所、库房的地理位置图、平面图（注明面积）、库房的产权证明及使用权证明复印件、（委托贮存的，应提交经营场所地理位置图、平面图（注明面积）和与被委托方签署的书面协议复印件、被委托方的《医疗器械经营许可证》复印件
ndled according to the Implementation Rules of BeijingMunicipality (2017 Revision), and the specific materials are asfollows: 1. Application Form for Business License of Medical Device(1 original) 2. Copy of Business License (original copy forinspection); (1 copy) 3. The legal representative, head of theenterprise, head of the quality certificate (check the original),certificate or title certificate copy (for unified purchasingchannels, take the chain enterprise headquarters qualitycertificate, copy of the title); (submit the original) (copy of 3copies) 4. Basic information of the enterprise (1 originalcopy).(Content contains: organization and department setinstructions, business premises, warehouse geographical locationmap, plan (indic
