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LEGIONELLA K-SET CORIS BIOCONCEPT - COFEPRIS Registration 2245R2018 SSA

Access comprehensive regulatory information for LEGIONELLA K-SET CORIS BIOCONCEPT (LEGIONELLA K-SET CORIS BIOCONCEPT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2245R2018 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on September 25, 2018.

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
2245R2018 SSA
LEGIONELLA K-SET CORIS BIOCONCEPT
COFEPRIS Analysis ID: 2245R2018 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA RรรDA DE DIAGNร“STICO IN VITRO PARA DETECCIร“N DE LEGIONELLA PNEUMOPHILIA LPS EN MUESTRAS DE ORINA

English

IN VITRO DIAGNOSTIC TEST FOR DETECTION OF LEGIONELLA PNEUMOPHILIA LPS IN URINE SAMPLES

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)
PRUEBA RยดยดAPIDA PARA LA DETECCIร“N DE LEGIONELLA PNEUMOPHILIA
Trade Name (English)
R ฬ ฬAPIDA TEST FOR THE DETECTION OF LEGIONELLA PNEUMOPHILIA
Registration Information
Analysis ID
2245R2018 SSA
Registration Date
September 25, 2018
Manufacturer / Fabricante
Name (English)
PHARMACUR, S.A. DE C.V.