2、相關(guān)部門受理申請(qǐng)人的申請(qǐng);

3、到實(shí)際場(chǎng)地進(jìn)行勘察以及對(duì)產(chǎn)品進(jìn)行審核;

4、準(zhǔn)予頒發(fā)三類醫(yī)療器械許可證。

以上就是對(duì)三類醫(yī)療器械經(jīng)營(yíng)許可證辦理的相關(guān)介紹，辦理的程序可能較為繁瑣。

如果您不知道自己的產(chǎn)品是什么類型的，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，庫房地址以及產(chǎn)品編號(hào)，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(yíng)業(yè)執(zhí)照正副本以及公章；

4.庫房地址材料；

applicant; 3. Investigate the actual site and audit the products; 4. Grant the issuance of a class III medical device license. The above is the relevant introduction of the three types of medical device business license processing, the procedures may be more cumbersome. If you 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. Lega