Mexico COFEPRIS registration 1671R2022 SSA

KIT PARA LA DETERMINACIÓN CUANTITATIVA DE LA PROTEÍNA C REACTIVA (CRP).

EN: KIT PARA LA DETERMINACIÓN CUANTITATIVA DE LA PROTEÍNA C REACTIVA (CRP).
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·KABLA COMERCIAL, S.A. DE C.V.·Registered December 16, 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® CRP KIT, CRP CONTROL M, CRP CALIBRADOR M.
Trade Name (English)
OMLIPO® CRP KIT, CRP CONTROL M, CRP CALIBRADOR M.
Registration information
Analysis ID
1671R2022 SSA
Registration Date
December 16, 2022
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for KIT PARA LA DETERMINACIÓN CUANTITATIVA DE LA PROTEÍNA C REACTIVA (CRP). (KIT PARA LA DETERMINACIÓN CUANTITATIVA DE LA PROTEÍNA C REACTIVA (CRP).) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1671R2022 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on December 16, 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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