醫(yī)療器械資質辦理流程

1.申請醫(yī)療器械生產(chǎn)許可證：申請者需向國家食品藥品監(jiān)管部門提交材料,，經(jīng)過審核,，如符合相關要求，會向申請者發(fā)放生產(chǎn)許可證,。

2.申請醫(yī)療器械注冊證：在擁有醫(yī)療器械生產(chǎn)許可證后,，申請者需要向國家食品藥品監(jiān)管部門提交醫(yī)療器械注冊申請材料，如通過審核,，會頒發(fā)醫(yī)療器械注冊證書,。

3.申請醫(yī)療器械市場許可證：擁有醫(yī)療器械注冊證后，申請者需要向所在區(qū)或市的食品藥品監(jiān)管部門申請市場許可證,，如通過審核,，會頒發(fā)市場許可證。

4.繳納相關費用：在獲得各類許可證后,，需要向相關機構繳納相應的證書費用和資料認證費用,。

5.領取證書：繳納證書費用后，即可領取醫(yī)療器械生產(chǎn)許可證,、醫(yī)療器械注冊證和市場許可證，正式開始運營,。

How to handle the business license of class III medical devices
1. The business license of Class III medical devices is handled as follows:
(1) The applicant shall submit the application materials to the relevant departments;
(2) Relevant departments shall accept the application of the applicant;
(3) Investigate the actual site and audit the products;
(4) Grant the issuance of a class III medical device license.

Three kinds of medical devices as the highest risk in the medical device classification category, strictly by the supervision and management, but for many families of three kinds of medical devices, many basic problems is not fully grasp, today we will take a look, what are three business scope of medical devices? How to apply for the three types of medical e business license again!