Costa Rica

Medical Device Consulting Services for Costa Rica

In order to register your medical device for sale in Costa Rica, you must first obtain approval for your product from the Costa Rican Ministry of Health. Appointing an in-country representative and properly classifying your device according to the Ministry of Health’s four-tier classification system are also required for market entry in Costa Rica.

From our office in San Jose, Emergo Group can fully support your registration effort in Costa Rica. We can address medical device classification and registration requirements put forth by the Ministry of Health and ensure a cost-effective and efficient path to market for your product in Costa Rica.