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MICROSCAN RAPID YEAST ID PANEL. - COFEPRIS Registration 2081R2019 SSA

Access comprehensive regulatory information for MICROSCAN RAPID YEAST ID PANEL. (MICROSCAN RAPID YEAST ID PANEL.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2081R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on November 05, 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
2081R2019 SSA
MICROSCAN RAPID YEAST ID PANEL.
COFEPRIS Analysis ID: 2081R2019 SSA
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Product Use / Uso del Producto
Spanish

PARA LA IDENTIFICACIÓN RÁPIDA DE LEVADURAS Y ESPECIES AFINES AISLADAS EN MUESTRAS CLÍNICAS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE.

English

FOR THE RAPID IDENTIFICATION OF YEASTS AND RELATED SPECIES ISOLATED IN CLINICAL SAMPLES. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR CLINICAL LABORATORY OR CABINET USE ONLY.

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)
REACTIVO PARA IDENTIFICACIÓN DE LEVADURAS.
Trade Name (English)
REAGENT FOR YEAST IDENTIFICATION.
Registration Information
Analysis ID
2081R2019 SSA
Registration Date
November 05, 2019
Manufacturer / Fabricante
Name (English)
BECKMAN COULTER DE MÉXICO, S.A. DE C.V.