INMUNOENSAYO DE QUIMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LOS NIVELES 25-HIDROXIVITAMINA D EN SUERO Y PLASMA HUMANO
Mexico·Clase I·III. Agentes de
diagnóstico·BECKMAN COULTER DE
MÉXICO, S.A. DE C.V.·Registered July 08, 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)
- ACCESS 25(OH) VITAMIN D TOTAL REAGENT & CALIBRATORS.
- Trade Name (English)
- ACCESS 25(OH) VITAMIN D TOTAL REAGENT & CALIBRATORS.
- Analysis ID
- 1927R2024 SSA
- Registration Date
- July 08, 2024
- Name (Spanish)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for INMUNOENSAYO DE QUIMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LOS NIVELES 25-HIDROXIVITAMINA D EN SUERO Y PLASMA HUMANO (INMUNOENSAYO DE QUIMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LOS NIVELES 25-HIDROXIVITAMINA D EN SUERO Y PLASMA HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1927R2024 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on July 08, 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.