PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA LIBRE (FT3).
Mexico·Clase I·III. Agentes de
diagnóstico·DRPRO MED S.A. DE C.V.·Registered February 09, 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)
- FREE TRIIODOTHYRONINE (CLIA) - WONDFO.
- Trade Name (English)
- FREE TRIIODOTHYRONINE (CLIA) - WONDFO.
- Analysis ID
- 0473R2024 SSA
- Registration Date
- February 09, 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 DE LA TRIYODOTIRONINA LIBRE (FT3). (PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA LIBRE (FT3).) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0473R2024 SSA and manufactured by DRPRO MED S.A. DE C.V.. The device was registered on February 09, 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.