Medical devices are officially regulated as “biomedical equipment and material” in Costa Rica. The Costa Rican Ministry of Health oversees the country’s medical device market, and subjects all devices except certain low-risk products to registration before commercialization can occur.
Through our worldwide network of consultants, industry contacts and regulatory sources, Emergo Group can provide in-depth analysis of all major medical device markets, including Costa Rica. Our Global Regulatory Overview Report service provides the following information:
If you would like to see what these reports include, you can download a sample Regulatory Overview Report.