医用外科口罩eua申请办理，医用外科口罩产品出口美国地区如果没有做510k测试需要做美国应急备案，就是美国eua申请办理事项，如有需求请联系咨询了解。
未在美国境内的上市的医疗用途的外科口罩、N95口罩，不管是美国境内还是境外制造商，都可以申请紧急授权。需要递交以下资料，并发送到FDA这个邮gicalMasks@fda.hhs.gov，由FDA审核是否可以授予紧急授权，让该产品在新冠疫情期间在美国境内销售。
资料如下：
1、General information such as your contact information, name andplace of business,email address, and contact information for a U.S.agent (if any) in addition to generalinformation about the devicesuch as the proprietary or brand name, model number,and marketingauthorization in your country (or region).
2、copy of the product labeling.
3、Whether the device currently has marketing authorization inanother regulatory jurisdiction (including certification number, ifavailable).
4、Whether the device is manufactured in compliance with 21 CFRPart 820 or ISO13485: Medical Devices – Quality Management Systems– Requirements forRegulatory Purposes or an equivalent qualitysystem and the manufacturer or importer has documentation ofsuch.
5、Description of testing conducted on the device, including anystandards met, such as
6、liquid barrier protection, flammability, biocompatibility, andfiltration performance, asappropriate. For surgical N95respirators, FDA recommends including fluid resistance testing(liquid barrier performance).
以上递交资料适用于本来就已经生产医疗器械、但口罩尚未在美国境内上市的制造商。有两点是需要注意的：
1、FDA只是减免了510（k）技术文档要求，但关于产品测试，生产车间质量体系的要求是从未有放弃的；
2、在新冠肺炎疫情爆发期间内，FDA不拘泥于任何区域的产品标准，只要你是做相关产品测试，欧盟的、中国的，都可以将测试报告递交，由FDA决定是否可以授予紧急授权。
FDA也欢迎非医疗器械企业生产销售医疗器械，可以粗暴理解成就是连生产车间QSR820都未外审过的制造商，至于要怎么操作，发邮件问FDA。
