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EMIT® 2000 TOBRAMICIN CALIBRATOR - COFEPRIS Registration 362R2019 SSA

Access comprehensive regulatory information for EMIT® 2000 TOBRAMICIN CALIBRATOR (EMIT® 2000 TOBRAMICIN CALIBRATOR) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 362R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on February 25, 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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COFEPRIS Official Data
Clase I
362R2019 SSA
EMIT® 2000 TOBRAMICIN CALIBRATOR
COFEPRIS Analysis ID: 362R2019 SSA
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Product Use / Uso del Producto
Spanish

CALIBRADOR DE TOBRAMICINA

English

TOBRAMYCIN CALIBRATOR

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)
CALIBRADOR DE TOBRAMICINA
Trade Name (English)
TOBRAMYCIN CALIBRATOR
Registration Information
Analysis ID
362R2019 SSA
Registration Date
February 25, 2019
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR