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C3 TURBITEST AA - COFEPRIS Registration 986R2019 SSA

Access comprehensive regulatory information for C3 TURBITEST AA (C3 TURBITEST AA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 986R2019 SSA and manufactured by REPRESENTACIONES LABIN MEXICO SA DE CV. The device was registered on May 13, 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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COFEPRIS Official Data
Clase I
986R2019 SSA
C3 TURBITEST AA
COFEPRIS Analysis ID: 986R2019 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DEL COMPONENTE C3 DEL COMPLEMENTO

English

REAGENT FOR THE DETERMINATION OF THE C3 COMPONENT OF COMPLEMENT

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACION DEL COMPONENTE C3 DEL COMPLEMENTO
Trade Name (English)
REAGENT FOR THE DETERMINATION OF THE C3 COMPONENT OF COMPLEMENT
Registration Information
Analysis ID
986R2019 SSA
Registration Date
May 13, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTATIONS LABIN MEXICO SA DE CV