Mexico COFEPRIS registration 1101R2019 SSA

AGAR DNASA CON TOLUIDINA MCD LAB.

EN: AGAR DNASA WITH TOLUIDINE MCD LAB.
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·MCD LAB, S.A. DE C.V.·Registered May 21, 2019
Product Use / Uso del Producto
Spanish

MEDIO DE CULTIVO PARA LA DIFERENCIACIÓN DE MICROORGANISMOS GRAM NEGATIVOS, PRINCIPALMENTE DE LOS GÉNEROS SERRATIA Y KLEBSIELLA, BASADOS EN LA ACTIVIDAD DE LA DESOXIRRIBONUCLEASA. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIO

English

CULTURE MEDIUM FOR THE DIFFERENTIATION OF GRAM-NEGATIVE MICROORGANISMS, MAINLY OF THE GENERA SERRATIA AND KLEBSIELLA, BASED ON THE ACTIVITY OF DEOXYRIBONUCLEASE. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR LABORATORY 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)
MEDIO DE CULTIVO.
Trade Name (English)
CULTURE MEDIUM.
Registration information
Analysis ID
1101R2019 SSA
Registration Date
May 21, 2019
Manufacturer / Fabricante
Name (Spanish)
MCD LAB, S.A. DE C.V.
Name (English)
MCD LAB, S.A. DE C.V.
About this record

Access comprehensive regulatory information for AGAR DNASA CON TOLUIDINA MCD LAB. (AGAR DNASA WITH TOLUIDINE MCD LAB.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1101R2019 SSA and manufactured by MCD LAB, S.A. DE C.V.. The device was registered on May 21, 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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