6．企業(yè)真實(shí)性保證材料（原件1份）。（內(nèi)容包含：申報(bào)材料真實(shí)性的自我保證聲明，并對(duì)材料作出如有虛假承擔(dān)法律責(zé)任的承諾、凡申請(qǐng)企業(yè)申報(bào)材料時(shí)，具體辦理人員不是法定代表人或負(fù)責(zé)人本人的，企業(yè)應(yīng)當(dāng)提交《授權(quán)委托書(shū)》

三類(lèi)醫(yī)療器械許可證經(jīng)營(yíng)范圍包括:醫(yī)用電子儀器設(shè)備，醫(yī)用光學(xué)器具、儀器及內(nèi)窺鏡設(shè)備，醫(yī)用磁共振設(shè)備，醫(yī)用X射線(xiàn)設(shè)備，手術(shù)室、急救室、診療室設(shè)備及器具。售賣(mài)醫(yī)療器械必須辦理經(jīng)營(yíng)許可

證，根據(jù)相關(guān)法律規(guī)定，國(guó)家食品藥品監(jiān)督管理局逐步推行醫(yī)療器械經(jīng)營(yíng)質(zhì)量規(guī)范管理制度。醫(yī)療器械經(jīng)營(yíng)質(zhì)量管理規(guī)范由國(guó)家食品藥品監(jiān)管管理局組織制定。

三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證辦理所需大致資料:

1、企業(yè)經(jīng)營(yíng)執(zhí)照;2、企業(yè)負(fù)責(zé)人以及質(zhì)檢人員和技術(shù)人員的身份、學(xué)歷、職稱(chēng)證明;3、經(jīng)營(yíng)場(chǎng)所證明以及地理位置圖。

三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證辦理之后需要明確的幾個(gè)注意事項(xiàng)

1、醫(yī)療器械經(jīng)營(yíng)許可證的有效期只有5年。有效期屆滿(mǎn)需要延續(xù)的，醫(yī)療器械經(jīng)營(yíng)企業(yè)應(yīng)當(dāng)在有效期屆滿(mǎn)6個(gè)月前，向原發(fā)證部門(mén)提出《醫(yī)療器械經(jīng)營(yíng)許可證》延續(xù)申請(qǐng)。

ical device license includes: medical electronic instruments and e, medical optical instruments, instruments and endoscope e, medical magnetic resonance e, medical X-ray e, operating room, emergency room, medical room e and e. The sale of medical devices must be applied for the business license Certificate, according to the relevant laws and regulations, the State Food and Drug Administration has gradually implemented the standard management system of medical device business. The management standards for medical devices shall be formulated by the State Food and Drug Administration. General information required for handling the business license of Class III medical devices: 1. Bu