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MEDIO DE CULTIVO - COFEPRIS Registration 0934R2024 SSA

Access comprehensive regulatory information for MEDIO DE CULTIVO (MEDIO DE CULTIVO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0934R2024 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on April 05, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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
0934R2024 SSA
MEDIO DE CULTIVO
COFEPRIS Analysis ID: 0934R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
BDTM BBLTM AGAR BILIS ESCULINA
Trade Name (English)
BDTM BBLTM AGAR BILIS ESCULINA
Registration Information
Analysis ID
0934R2024 SSA
Registration Date
April 05, 2024
Manufacturer / Fabricante
Name (English)
BECTON DICKINSON DE MÉXICO, S.A. DE C.V.