出口日本的PMDA注冊(cè)醫(yī)療器械公司希望把產(chǎn)品投放到日本市場(chǎng)必須要滿足日本的Pharmaceutical and Medical Device Act (PMD Act)，在PMD Act的要求下，TOROKU注冊(cè)系統(tǒng)要求國(guó)外的制造商必須向PMDA注冊(cè)制造商信息。包裝上印有ウィルスカット99%的字?樣?都是超過(guò)國(guó)內(nèi)過(guò)濾效率95%（N95口罩）標(biāo)準(zhǔn)的醫(yī)用口罩!

1. 醫(yī)用防護(hù)口罩：符合中國(guó)GB 強(qiáng)制性標(biāo)準(zhǔn)，過(guò)濾效率≥95%（使用非油性顆粒物測(cè)試）。

2. N95口罩：美國(guó)NIOSH認(rèn)證，非油性顆粒物過(guò)濾效率≥95%。

3. KN95口罩：符合中國(guó)GB 2626 強(qiáng)制性標(biāo)準(zhǔn)，非油性顆粒物過(guò)濾效率≥95%歐盟

4、必要資料（資質(zhì)）

提單，箱單

5、在歐盟，口罩屬于PPE個(gè)人防護(hù)用品，“危及健康的物質(zhì)和混合物”。2019年起，歐盟新法規(guī)PPE Regulation (EU) 2016/425強(qiáng)制執(zhí)行，所有出口歐盟的口罩必須在新法規(guī)的要求下獲得CE認(rèn)證證書(shū)。CE認(rèn)證是歐盟實(shí)行的強(qiáng)制性產(chǎn)品安全認(rèn)證制度，目的是為了保障歐盟國(guó)家人民的生命財(cái)產(chǎn)安全。

美國(guó)目前并沒(méi)有官方禁止口罩出口的消息。建議中國(guó)賣(mài)家及時(shí)關(guān)注國(guó)內(nèi)外防疫物資出口資質(zhì)認(rèn)證和監(jiān)管要求，避免造成產(chǎn)品被扣押和退回的風(fēng)險(xiǎn)。屬于醫(yī)療器械類(lèi)的口罩，不同國(guó)家的資質(zhì)和要求都不相同，這點(diǎn)賣(mài)家們一定要注意。

1. Medical protective mask: comply with Chinese GB compulsory standard, with filtration efficiency ≥ 95% (test with non oily particles).

2. N95 respirator: NIOSH certified, the filtration efficiency of non oil particles ≥ 95%.

3. Kn95 respirator: it meets the mandatory standard of China GB 2626, and the filtration efficiency of non oil particles ≥ 95% of EU

4. Necessary inbation (qualification)

Bill of lading, packing list, invoice

5. In the European Union, masks are PPE personal protective equipment, "substances and mixtures dangerous to health". From 2019, the new EU regulation PPE regulation (EU) 2016 / 425 is enforced. All masks exported to the EU must obtain CE certification under the requirements of the new regulation. CE certification is a compulsory product safety certification system implemented by EU, which aims to protect the life and property safety of EU people.

There is no official ban on the export of masks in the United States. It is suggested that Chinese sellers should pay attention to the export qualification certification and regulatory requirements of domestic and foreign anti epidemic materials in time to avoid the risk of product seizure and return. The qualification and requirements of respirators belonging to medical devices are different in different countries. The sellers must pay attention to this.

李國(guó)杰（經(jīng)理） ：18202125732 

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