PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS
Mexico·Clase I·III. Agentes de
diagnóstico·DRPRO MED S.A. DE C.V.·Registered July 02, 2024- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- D-DIMER (CLIA) - WONDFO
- Trade Name (English)
- D-DIMER (CLIA) - WONDFO
- Analysis ID
- 1855R2024 SSA
- Registration Date
- July 02, 2024
- Name (Spanish)
- DRPRO MED S.A. DE C.V.
- Name (English)
- DRPRO MED S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS (PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL DÍMERO D CIRCULANTE EN EL PLASMA Y SANGRE HUMANOS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1855R2024 SSA and manufactured by DRPRO MED S.A. DE C.V.. The device was registered on July 02, 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.