Mexico COFEPRIS registration 1468R2022 SSA

PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL INACTIVADOR C1 (C1IN)

EN: PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL INACTIVADOR C1 (C1IN)
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·KABLA COMERCIAL, S.A. DE C.V.·Registered November 28, 2022
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
OMLIPO C1IN KIT (C1 INACTIVADOR)
Trade Name (English)
OMLIPO C1IN KIT (C1 INACTIVADOR)
Registration information
Analysis ID
1468R2022 SSA
Registration Date
November 28, 2022
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL INACTIVADOR C1 (C1IN) (PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DEL INACTIVADOR C1 (C1IN)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1468R2022 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on November 28, 2022.

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.

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