医疗器械产品的授权书LOA证书，企业出口医疗器械产品的时候所授权给进口商代理销售的证书资料。几乎是医疗器械产品的进口商都会要求提供自由销售证书FSC以及LOA授权委托书，这是基本的资料，清关资料需要进口国的驻华大使馆加签，更加的具有影响力。授权书LOA使馆加签怎么办理，什么是授权书LOA，使馆加签还需要什么资料。。
importers of medical device products will require to provide free sales certificate FSC and LOA power of attorney, which is the basic information, customs clearance information needs to be signed by the embassy of the importing country in China, more influential.
—— 医疗器械产品授权书LOA的使馆加签办理资料。
解：医疗器械产品授权书LOA的使馆加签需要有英文，大多进口商规定医疗器械产品授权书LOA的使馆加签上需要有当地的译文，使馆公证需要有英文翻译件， 使馆加签的资料跟其他的资料一样，具体咨询管理员。
The embassy signature of the medical device product authorization LOA needs to be in English. Most importers require that the embassy signature of the medical device product authorization LOA needs to have a local translation, and the embassy notarization needs to have an English translation
—— 医疗器械产品授权书LOA的填写规范。
解：医疗器械产品授权书LOA的格式通常如下：我司***兹授权***公司在**的特约经销商，负责我单位生产的***产品在**地区的销售事宜。文件上的内容是需要有英文以及当地的语言（西文或越南文等）翻译。
—— 医疗器械产品授权书LOA是怎么样的一份文书。。
解： 医疗器械产品授权书LOA (Letter of Authorization)即授权函，生产企业提供给销售企业的一份文书，生产企业授把生产的产品授权给销售企业进行销售。LOA是一份重要的文件，其有效性和可被承认与否，关系到销售企业是否具备合法、有权代理产品销售的资格。
LOA is a document provided by a production company to a sales company, and the production company grants the production product to the sales company for sale.
医疗器械产品授权书LOA想要更加具有时效性，需要有进口国的驻华大使馆加签双认证—外交部和使馆的双重认证。双重认证确保了文件在进口国的合法性以及有效性。日常的医疗器械产品出口需要的资料有【LOA】以及【产品注册证】、 【Letter of Warranty 】等文件。医疗器械产品授权书，授权书LOA办理资料，LOA领事馆加签双认证。
Dual certification by the Embassy of the importing country in China - dual certification by the Ministry of Foreign Affairs and the Embassy. Two-factor authentication ensures the legitimacy and validity of documents in the importing country. The documents required for daily export of medical device products include [LOA], [Product Registration Certificate], [Letter of Warranty] and other documents