根據(jù)《醫(yī)療器械監(jiān)督管理?xiàng)l例》第三十一條的規(guī)定，從事第三類醫(yī)療器械業(yè)務(wù)的，經(jīng)營(yíng)企業(yè)應(yīng)當(dāng)向所在地設(shè)區(qū)的市級(jí)人民政府食品藥品監(jiān)督管理部門申請(qǐng)經(jīng)營(yíng)許可。

1.有與經(jīng)營(yíng)范圍相適應(yīng)的營(yíng)業(yè)場(chǎng)所和倉(cāng)庫，并有特定的面積要求；

2.具有國(guó)家認(rèn)可的專門從事產(chǎn)品經(jīng)營(yíng)的在職人員；

3、應(yīng)有具有中專以上學(xué)歷的與產(chǎn)品管理相關(guān)的技術(shù)人員；

4.具有與所經(jīng)營(yíng)的醫(yī)療器械相適應(yīng)的質(zhì)量管理體系。

許可證的所需材料

1.營(yíng)業(yè)執(zhí)照；

2.企業(yè)負(fù)責(zé)人、質(zhì)量檢驗(yàn)人員和技術(shù)人員的身份、學(xué)歷和職稱證明；

3.營(yíng)業(yè)場(chǎng)所證明和地理位置圖。

辦理后的注意事項(xiàng)

ndary school education or above; 4. Have a management system suitable for the medical devices it operates. Materials required for the permit 1. Business license; 2. The identity, educational background and professional title certificate of the person in charge of the enterprise, the inspection personnel and the technical personnel; 3. Business site certificate and geographical location map. Matters needing attention after handling