北京第二类医疗器械备案定义

北京第二类医疗器械备案是从事第二类医疗器械经营的，经营企业应填写第二类医疗器械经营备案表，向所在地设区的市级食品药品监督管理部门备案，并提交符合第二类医疗器械经营备案材料要求的备案材料.

北京第二类医疗器械备案办理流程

签署合同——支付预付款——公司查名——准备材料——向当地药检局递交申请材料——通过药检局检查——获得《医疗器械经营许可证》——注册资金到位——获得营业执照——获得组织机构代码证——获得税务登记证——交付材料、支付余款——结束

How long does it take to approve the registration of the class III medical device license? (1) Acceptance: The applicant shall apply to the Administrative Acceptance Service Center, submit the application materials in accordance with the catalogue listed in Article 6 of the Instructions, and the staff of the Acceptance Center shall examine the application materials in accordance with the requirements of the Acceptance Standards for the Registration and Application Materials of Domestic Third Class and Overseas Medical Devices (National Drug Administration [2005] No.111). Where the application item does not need to obtain an administrative license according to law, The applicant shall be informed immediately of the non-acceptance of the application; Where the application items do not fall within the scope of the functions and powers of the administrative organ according to law, A decision shall be made immediately, And inform the applicant to apply to the relevant administrative organ;