Mexico
Medical electrical equipment (MEE) has their own requirements for safety and performance due to the nature of the electrical/electronic systems involved. In the case
As mentioned in our Classification and Grouping Guide, there are a series of rules to consider when classifying and grouping medical devices. The above-mentioned rules
The Certificate of Free Sale (CFS), also known as “Certificate for Export” or “Certificate to Foreign Government”, is a document to evidence that goods, such
Last May the 31st 2021, the Ministry of Health in Mexico released an update to the Health Supplies Regulation. There are several amendments impacting different
Technological advances in health care have positioned software as an essential component of products and services for the diagnosis and analysis of clinical conditions and diseases. Although software
The market of previously owned medical devices in Mexico works in different business models and therefore, arises questions about its regulatory requirements. For instance, public
