Mexico COFEPRIS registration 917R2019 SSA

AGAR MUELLER HINTON CON 5% DE SANGRE DE CARNERO MCD LAB

EN: AGAR MUELLER HINTON WITH 5% RAM BLOOD MCD LAB
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·MCD LAB, S.A. DE C.V.·Registered May 03, 2019
Product Use / Uso del Producto
Spanish

EL AGAR MUELLER HINTON ADICIONADO CON SANGRE ES UTILIZADO PARA PRUEBAS DE SUSCEPTIBILIDAD ANTIMICROBIANA DE STREPTOCOCCUS PNEUMONIAE. AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETE.

English

MUELLER HINTON AGAR ADDED WITH BLOOD IS USED FOR ANTIMICROBIAL SUSCEPTIBILITY TESTING OF STREPTOCOCCUS PNEUMONIAE. IN VITRO DIAGNOSTIC AGENT. FOR USE IN CLINICAL OR CABINET LABORATORIES 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 PREPARADO
Trade Name (English)
PREPARED CULTURE MEDIUM
Registration information
Analysis ID
917R2019 SSA
Registration Date
May 03, 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 MUELLER HINTON CON 5% DE SANGRE DE CARNERO MCD LAB (AGAR MUELLER HINTON WITH 5% RAM BLOOD 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 917R2019 SSA and manufactured by MCD LAB, S.A. DE C.V.. The device was registered on May 03, 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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