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

辦理二類備案您需要提供：

1.法人身份信息；

2.質(zhì)量員身份信息；

3.公司營業(yè)執(zhí)照正副本以及公章；

4.庫房地址材料；

三類醫(yī)療器械經(jīng)營許可證辦理流程

一、要網(wǎng)登，申請醫(yī)療器械經(jīng)營許可證填寫公司相關(guān)資料并提交。

二、提交完畢后需要準備以下資料去現(xiàn)場提交材料

1.）《醫(yī)療器械經(jīng)營許可證申請表》

2）《營業(yè)執(zhí)照正副本原件)(復印件)

3）法定代表人、企業(yè)負責人、質(zhì)量負責人的身份證明、學歷或者職稱證明復印件；

4.）組織機構(gòu)與部門設(shè)置說明

5）經(jīng)營場所、庫房地址的地理位置圖、平面圖、房屋產(chǎn)權(quán)證明文件或者由房屋租賃所出具的房屋租賃憑證復印件,屬倉儲委托區(qū)療器械第三方物流的,提供委托合同(復印件1份,).

ersonnel, 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, 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, apply for the medical device business license to fill in the company's relevant information and submit. 2. After the submission, the next step needs to prepare the following materials to submit the materials on site 1.) Application Form for Medical Device Business License 2) Original copy of the business License) (photocopy) 3) Copy of the identity certificate, educational background or professional title certificate of the legal representative, the