丰台六里桥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库房速度快专业方便。
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一、三类医疗器械经营许可证如何办理
1、很多药品或者医疗器械的经销商,如果没有三类医疗器械经营许可证,很多产品就不能卖,比如说体外诊断试剂就属于三类医疗器械,只有有相关证书,才能销售这种产品。
2、要办理三类医疗器械经营许可证,必须有相关的营业执照,一般营业执照上的经营范围这一栏,需要明确写道可以销售三类医疗器械。如果没有,需要去工商局办理增项。
3、销售三类医疗器械,你必须要自己的库房,而且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,所以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,然后领取《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。
二、经营许可证是营业执照吗
二者不能等同。
根据法律规定,营业执照是法律主体进行市场交易主体资格的法定证明,目前有法人类营业执照、个人独资企业营业执照、合伙企业营业执照和个体工商户营业执照等;营业执照由工商局颁发,每年年检。而经营许可证,是法律规定的某些行业必须经过许可,而由主管部门办法的许可经营的证明,如烟草专卖许可等。营业执照是每个开门做生意的经营者都需要办理的证件,没有这个证件,就是无照经营行为,是违法的。经营许可证是做某种方面的生意所必须取得的证件,这个证件必须在办理营业执照之前取得,也就是所谓的前
ercial bureau to check the warehouse, you would like to clean up the warehouse, and then get the "medical device business enterprise license application form" and fill in, and bring all the relevant qualifications of the enterprise, but also need to bring the relevant information of quality personnel. 5. The business license of Class III medical devices needs to be handled directly by the food and drug supervision and administration department of the municipal people's government, and shall be reviewed within 30 days after receiving the materials. If the relevant regulations are met, the business license of Class III medical devices can be issued. 2. Is the business license a business license The two cannot be equal. According to the law, the business license is the legal certificate of the qualification of the legal subject for market transaction. At present, there are legal human business license, business license, sole proprietorship business license, partnership business license and individual business license, etc. The business license is issued by the Industrial and Commercial Bureau for annual inspec