醫療器械經營許可證現為后置審批，有效期為5年。有效期屆滿需要延續的，依照有關行政許可的法律規定辦理延續手續。

一、三類醫療器知械許可證注冊所需材料

1、企業名稱與經營范圍，注冊資本及股東出資比例，股東等身份證明;

2、醫療器械產品注冊證書、供應商營業執照、許可證及授權書;

3、質量管理文件等;

4、2個或以上醫學專業或相關專業人員證書、身份證明與簡歷;

5、符合醫療器械經營要求的辦公場地及倉庫證明;

6、公司章程、股東會決議等;

7、財務人員身份證和上崗證;

8、其它相道關材料。

二、辦理三回類醫療器械許可證的要求：

1、場地要求：必須是辦公性質，使用面積要少達到45平方米;

2、人員要求：需要有3名相關人員(公司負責人、質量負責人、質量檢查人員)的備案并且持有證書;

3、產品要求：必須要有合乎業務范圍的產品信息，并出具證書;

4、其他相關法律法規要求。

ll be handled in accordance with the relevant legal provisions of the administrative license. 1. Materials required for the registration of class III medical e knowledge and device license 1. Enterprise name and business scope, registered capital and proportion of shareholder contribution, shareholders and other identity certificates; 2. Medical device product registration certificate, supplier business license, license and authorization letter; 3. management documents, etc.; 4,2 or more certificates, identification certificate and resume of medical professionals or related professionals; 5. Office space and warehouse certificate that meet the business re of medical e; 6. Articles of association, resolutions of shareholders' meeting, etc.; 7. ID card and post card of financial personnel; 8, other phase channel clearance materials. 2. Re for three-of medical device license: 1, site re: must be office nature, the use area should be less than 45 square meters; 2. Personnel re: 3 relevant personnel (company responsible person, qu