產(chǎn)品詳情
1、生產(chǎn)企業(yè)營業(yè)執(zhí)照
2、醫(yī)療器械注冊證
3、醫(yī)療物資聲明（表格不能留空，表頭不要有模板兩個字，蓋經(jīng)營單位公章）
4、醫(yī)療器械經(jīng)生產(chǎn)許可證
5、廠家的檢測合格報告(最好提供，以便查驗）
6、生產(chǎn)廠家及注冊證商品名稱，型號要對應(yīng)報關(guān)單信息，生產(chǎn)公司需要在海關(guān)名冊內(nèi)（注冊號要在藥監(jiān)局網(wǎng)上能查到此生產(chǎn)公司的信息才有效）
7、貨物里面的每個小包/盒都要有合格證（必須蓋章），產(chǎn)品或包裝或合格證上必須要有：
執(zhí)行標(biāo)準(zhǔn)，生產(chǎn)批次，廠商名稱，廠商地址，生產(chǎn)日期，有效期，醫(yī)療器械注冊證號，醫(yī)療器械許可證號（缺一不可）
1. Business license of production enterprise
2. Medical device registration certificate
3. Statement of medical materials (the b cannot be left blank, the header should not have two words of template, with the official seal of the business unit)
4. Production license of medical devices
5. Manufacturer's inspection report (preferably provided for inspection)
6. The name and model of the manufacturer and registered certificate shall correspond to the customs declaration inbation, and the production company shall be in the customs register (the registration number shall be valid only when the inbation of the production company can be found on the website of the drug administration)
7. Each small package / box in the goods shall have a certificate of conbity (which must be sealed), and the product or package or certificate of conbity must have:
Executive standard, production batch, manufacturer's name, manufacturer's address, production date, validity period, medical device registration certificate No., medical device license No. (one is indispensable)
李國杰（經(jīng)理）：18202125732
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