1.我要同時出口到日本和韓國，一定要符合他們國家的標準嗎？標準分別是什么？

回答：是的，一定要符合其他國家的標準，不然是進不去的。

出口日本要在PMD Act的要求下，TOROKU注冊系統要求國外的制造商必須向PMDA注冊制造商信息。

出口韓國需要標注原產地，并且需要有KF認證。

出口美國的口罩，必須有FDA認證。

出口歐洲的口罩必須有CE認證。

Answer: Yes, we must meet the standards of other countries, or we will not be able to enter.

To export to Japan at the request of PMD act, toroku registration system requires foreign manufacturers to register manufacturer inbation with PMDA.

Export to South Korea needs to be marked with origin and KF certification.

Masks exported to the United States must be FDA certified.

Masks exported to Europe must have CE certification.

2.現在我們的公司想要出口一批涉證口罩，不過沒有出口資質，想問一下還能進行出口嗎？

回答：如果是具備三證的工廠的產品，可以通過外貿代理進行出口銷售。如果沒有三證的話，那就不能出口了。

Answer: if it is a factory product with three certificates, it can be exported and sold through a foreign trade agent. If we don't have three certificates, we can't export them.

3.普通口罩和醫用口罩出口分別需要什么資質，需要辦理哪些證呢？

回答：普通和醫用，是指用途。而藥監局管理是按照產品品質和標準來管理的。二類和三類的醫療器械的口罩，需要備案證或者注冊證，才能出口。涉證的三證，見第2個問題的答案。

Answer: common and medical use refers to use. The administration of FDA is based on product quality and standards. The masks of class II and class III medical devices can only be exported if they need a registration certificate or registration certificate. For the three evidences involving evidence, see the answer to the second question.

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