Mexico COFEPRIS registration 1783R2024 SSA

INMUNOENSAYO QUIMIOLUMINISCENTE PARA LA DETECCIÓN CUALITATIVA DE ANTÍGENO DE HELICOBACTER PYLORI.

EN: INMUNOENSAYO QUIMIOLUMINISCENTE PARA LA DETECCIÓN CUALITATIVA DE ANTÍGENO DE HELICOBACTER PYLORI.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·KABLA COMERCIAL, S.A. DE C.V.·Registered June 25, 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)
HELICOBACTER PYLORI AG VIRCLIA® MONOTEST.
Trade Name (English)
HELICOBACTER PYLORI AG VIRCLIA® MONOTEST.
Registration information
Analysis ID
1783R2024 SSA
Registration Date
June 25, 2024
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for INMUNOENSAYO QUIMIOLUMINISCENTE PARA LA DETECCIÓN CUALITATIVA DE ANTÍGENO DE HELICOBACTER PYLORI. (INMUNOENSAYO QUIMIOLUMINISCENTE PARA LA DETECCIÓN CUALITATIVA DE ANTÍGENO DE HELICOBACTER PYLORI.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1783R2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on June 25, 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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