LÁSER DE DIODO. - COFEPRIS Registration 0148E2024 SSA

Access comprehensive regulatory information for LÁSER DE DIODO. (LÁSER DE DIODO.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0148E2024 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on January 17, 2024.

This page provides complete registration details including product type (I. Equipo Médico), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.