MICROSCAN RAPID YEAST ID PANEL.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·BECKMAN COULTER DE MÉXICO, S.A. DE C.V.·Registered November 05, 2019PARA 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.
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.
- 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.
- Analysis ID
- 2081R2019 SSA
- Registration Date
- November 05, 2019
- Name (Spanish)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
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.