2、相關(guān)部門(mén)受理申請人的申請;

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

4、準予頒發(fā)三類(lèi)醫療器械許可證。

以上就是對三類(lèi)醫療器械經(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(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(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