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(xún)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、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、提交完畢后需要準(zhǔn)備以下資料去現(xiàn)場(chǎng)提交材料

an 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. Copy of the business license 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, apply for the medical device business license to fill in the company's relevant information and submit. 2. After the submission, the ne