医疗器械墨西哥大使馆认证自由销售的条件

驻华大使馆认证 / 领事馆认证 /贸促会认证 /香港商会认证 /香港海牙认证 /原产地证--

想在墨西哥销售您的医疗器械产品？

墨西哥是一个开拓美国和欧盟的跳板，大多数医疗器械从这里出口到美国和欧盟。然而，注册流程并不简单。

墨西哥提供各种注册通道，每种通道均有制造商需要考虑的优势和劣势。以下就是比较通用的注册流程：

医疗器械产品在墨西哥注册登记流程：

准备材料：

FSC自由销售证书；

GMP证书；

ISO-13485；

代表函；格式参考如下：

Want to sell your medical devices in Mexico?

Mexico is a launching pad for the United States and The European Union, from where most medical equipment is exported. However, the registration process is not simple.

Mexico offers a variety of registered channels, each with advantages and disadvantages that the manufacturer needs to consider. Here is a more general registration process:

Procedures for the registration of medical devices in Mexico:

Preparation materials:

FSC Free Sale Certificate;

GMP certificate;

ISO - 13485;

On behalf of the letter; The format is as follows