办理流程是什么？
有与经营的第三类医疗器械相适应的营业场所和仓储场所，并提供经营场地的产权证明或者租赁合同；
有与经营的第三类医疗器械相适应的质量管理制度；
具有与经营的第三类医疗器械相适应的专业指导、技术培训和售后服务的能力，或者相关协议；
具有与经营的第三类医疗器械相适应的质量管理机构或者人员，质量管理人员应当具有国家认可的相关专业学历或者职称；
有能够保证医疗器械安全有效的质量管理体系；
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