INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE
Mexico·Clase I·III. Agentes de
diagnóstico·KABLA COMERCIAL, S.A.
DE C.V.·Registered April 17, 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)
- FOLLICLE-STIMULATING (ELECTROCHEMILUMINESC ENCE INMUNOASSAY) LIFOTRONIC
- Trade Name (English)
- FOLLICLE-STIMULATING (ELECTROCHEMILUMINESC ENCE INMUNOASSAY) LIFOTRONIC
- Analysis ID
- 1070R2024 SSA
- Registration Date
- April 17, 2024
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
Access comprehensive regulatory information for INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE (INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1070R2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on April 17, 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.