如果您不知道自己的產(chǎn)品是什么類(lèi)型的，可以打隨時(shí)咨詢我，可以給您妥善的建議,。

辦理醫(yī)療資質(zhì)許可證,，您需要具有相關(guān)的人員，庫(kù)房地址以及產(chǎn)品編號(hào),，我司均可以為您提供,。

辦理二類(lèi)備案您需要提供：

1.法人身份信息；

2.質(zhì)量員身份信息,；

3.公司營(yíng)業(yè)執(zhí)照正副本以及公章,；

4.庫(kù)房地址材料；

三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證辦理流程

一,、首先要網(wǎng)登,，申請(qǐng)醫(yī)療器械經(jīng)營(yíng)許可證填寫(xiě)公司相關(guān)資料并提交。

二,、提交完畢后接下來(lái)需要準(zhǔn)備以下資料去現(xiàn)場(chǎng)提交材料

 do not know what kind of product is, you can call me at any time, you can give you proper advice. For the medical license, you need to have the relevant personnel, warehouse address and product number, our company can provide it for you. For Class II filing, you need to provide: 1. Legal person identity information; 2. Identity information of the personnel; 3. The Company's business license principal and secondary copy and official seal; 4. Warehouse address materials; Procedures for handling the business license of Class III medical devices 1. First of all, to network access