TUBOS DE EXTRACCIÓN DE SANGRE DE UN SOLO USO EDTA K2/EDTA K3 - COFEPRIS Registration 0620R2024 SSA

Access comprehensive regulatory information for TUBOS DE EXTRACCIÓN DE SANGRE DE UN SOLO USO EDTA K2/EDTA K3 (TUBOS DE EXTRACCIÓN DE SANGRE DE UN SOLO USO EDTA K2/EDTA K3) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0620R2024 SSA and manufactured by DRPRO MED S.A. DE C.V.. The device was registered on March 05, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.