Mexico COFEPRIS registration 0005R2024 SSA

REACTIVO Y CONTROL PARA LA DETECCIÓN CUANTITATIVA PARA MEDIR EL DÍMERO D

EN: REACTIVO Y CONTROL PARA LA DETECCIÓN CUANTITATIVA PARA MEDIR EL DÍMERO D
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·KANA UNDESA, S.A. DE C.V.·Registered January 04, 2024
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)
STANDARD™ F D-DIMER
Trade Name (English)
STANDARD™ F D-DIMER
Registration information
Analysis ID
0005R2024 SSA
Registration Date
January 04, 2024
Manufacturer / Fabricante
Name (English)
KANA UNDESA, S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO Y CONTROL PARA LA DETECCIÓN CUANTITATIVA PARA MEDIR EL DÍMERO D (REACTIVO Y CONTROL PARA LA DETECCIÓN CUANTITATIVA PARA MEDIR EL DÍMERO D) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0005R2024 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on January 04, 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.

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