AGAR SALMONELLA-SHIGELLA/AGAR VERDEBRILLANTE.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MCD LAB, S.A. DE C.V.·Registered February 28, 2020ELAGARSALMONELLA-SHIGELLA/AGARVERDEBRILLANTE, ES UN MEDIO DE CULTIVOSELECTIVO Y DIFERENCIAL PRINCIPALMENTEPARA ENTEROBACTERIAS LACTOSA NEGATIVA.PARA USO EXCLUSIVO DE LABORATORIOCLÍNICO O DE GABINETE.
ELAGARSALMONELLA-SHIGELLA/BRIGHT GREEN AGAR, IS A SELECTIVE AND DIFFERENTIAL CULTURE MEDIUM MAINLY FOR LACTOSE-NEGATIVE ENTEROBACTERIACEAE. 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)
- MEDIO SELECTIVO Y DIFERENCIALPARA ENTEROBACTERIASPATÓGENAS.
- Trade Name (English)
- SELECTIVE AND DIFFERENTIAL MEDIUM FOR ENTEROBACTERIASPATHOGENES.
- Analysis ID
- 249R2020 SSA
- Registration Date
- February 28, 2020
- Name (Spanish)
- MCD LAB, S.A. DE C.V.
- Name (English)
- MCD LAB, S.A. DE C.V.
Access comprehensive regulatory information for AGAR SALMONELLA-SHIGELLA/AGAR VERDEBRILLANTE. (SALMONELLA-SHIGELLA AGAR/VERDEBRILLANTE AGAR.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 249R2020 SSA and manufactured by MCD LAB, S.A. DE C.V.. The device was registered on February 28, 2020.
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.