商局办理增项。
3、销售三类医疗器械，你必须要自己的库房，库房里需要设置冷藏库，因为三类医疗器械，是有保温需要的，超过一定的温度，就容易变质影响产品质量，很少有经销商有销售三类医疗器械的资格。
4、去工商局办理增项，是需要带着工商局的工作人员来查看库房的，你zui好把库房收拾一下，领取《医疗器械经营企业许可申请表》并填写，并把企业相关资质全部带上，还需要带上质量人员的相关资料。
5、三类医疗器械经营许可证，需要直接去市级人民政府食品药品监督管理部门办理，在接受资料后的30天内进行审核，如果符合相关规定，就可以颁发三类医疗器械经营许可证。
te and affect the quality of products, so few dealers arequalified to sell the third class of medical devices. 4, go to theindustrial and commercial Bureau for additional items, is the needto take the staff of the industrial and commercial bureau to checkthe warehouse, you would like to clean up the warehouse, and thenget the "medical device business enterprise license applicationform" and fill in, and bring all the relevant qualifications of theenterprise, but also need to bring the relevant information ofquality personnel. 5. The business license of Class III medicaldevices needs to be handled directly by the food and drugsupervision and administration department of the municipal people'sgovernment, and shall be reviewed within 30 days after receivingthe materials. If the relevant regulations are met,
