庫、出庫，實(shí)現(xiàn)產(chǎn)品在流通環(huán)節(jié)可追溯。

醫(yī)療器械經(jīng)營許可證申請須知

醫(yī)療器械經(jīng)營許可證是醫(yī)療器械經(jīng)營企業(yè)必須具備的，開辦第二類醫(yī)療器械經(jīng)營企業(yè)，應(yīng)當(dāng)向省、自治區(qū)、直轄市人民政府藥品監(jiān)督管理部門備案；

開辦第三類醫(yī)療器械經(jīng)營企業(yè)，應(yīng)當(dāng)經(jīng)省、自治區(qū)、直轄市人民政府藥品監(jiān)督管理部門審查批準(zhǔn)，并發(fā)給《醫(yī)療器械經(jīng)營許可證》。

依據(jù)《醫(yī)療器械經(jīng)營監(jiān)督管理辦法》，開設(shè)三類醫(yī)療器械運(yùn)營公司，食品類藥品監(jiān)督管理局單位將會對經(jīng)營地開展當(dāng)場審查。對不符合要求標(biāo)準(zhǔn)的，明確提出整頓規(guī)定或未予批準(zhǔn)。根據(jù)《藥品醫(yī)療器械飛行檢查辦法》，食品類藥品監(jiān)督管理局單位將會對醫(yī)療機(jī)械銷貨方式合理合法、工作人員在職人員在職、拿貨檢查、運(yùn)送儲存等層面開展不事先告之的監(jiān)督管理。三類醫(yī)療器械的界定

依據(jù)《醫(yī)療器械監(jiān)督管理?xiàng)l例》，第三類醫(yī)療器械是具備較高危，必須采用非常對策嚴(yán)控管理方法以確保其安全性、合理的醫(yī)療機(jī)械。例如普遍的注射器、注射針、靜脈留置針、心臟支架、麻醉機(jī)、CT、磁共振等。

申請辦理三類醫(yī)療器械許可證必須提前準(zhǔn)備的原材料

（1）企業(yè)營業(yè)執(zhí)照；

（2）公司章；

（3）房屋產(chǎn)權(quán)證明、租賃協(xié)議；

（4）法定代表人、主要負(fù)責(zé)人、品質(zhì)管理員的身份、畢業(yè)證等證明材料；

（5）經(jīng)營地平面設(shè)計(jì)圖，倉庫平面設(shè)計(jì)圖。

申請辦理三類醫(yī)療器械許可證的規(guī)定

（1）場所和倉庫總面積規(guī)定：與經(jīng)營地企業(yè)規(guī)模相一致。

nicipality directly under the Central Government; The establishment of a class III medical device trading enterprise shall be examined and approved by the drug regulatory department of the people's government of the province, autonomous region or municipality directly under the Central Government, and a Medical Device Trading License shall be issued. According to the Measures for Supervision and Administration of Medical Device Operation, the third type of medical device operating company will be established, and the food and Drug Administration will carry out on-the-spot examination of the place of operation. For those that do not meet the re, the rectification provisions shall be clearly prescribed or shall not be approved. According to the Measures for Flight Inspection of Drugs and Medical Devices, the Food and Drug