Mexico COFEPRIS registration 2159R2019 SSA

BIO- CLOSTRIDIUM

EN: BIO- CLOSTRIDIUM
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·QUIMIBIOL, S.A. DE C.V.·Registered November 19, 2019
Product Use / Uso del Producto
Spanish

PRUEBA PARA LA DETECCIÓN CUALITATIVA DE CLOSTRIDIUM DIFFICILE EN HECES

English

TEST FOR THE QUALITATIVE DETECTION OF CLOSTRIDIUM DIFFICILE IN FECES

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
PRUEBA PARA DETECCIÓN DEL ANTÍGENO CLOSTRIDIUM DIFFICILE
Trade Name (English)
CLOSTRIDIUM DIFFICILE ANTIGEN TEST
Registration information
Analysis ID
2159R2019 SSA
Registration Date
November 19, 2019
Manufacturer / Fabricante
Name (English)
QUIMIBIOL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for BIO- CLOSTRIDIUM (BIO- CLOSTRIDIUM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2159R2019 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on November 19, 2019.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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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