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FLUJOMETRO - COFEPRIS Registration 0635E2024 SSA

Access comprehensive regulatory information for FLUJOMETRO (FLUJOMETRO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0635E2024 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on March 05, 2024.

This page provides complete registration details including product type (I. Equipo Mรฉdico), 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 II
0635E2024 SSA
FLUJOMETRO
COFEPRIS Analysis ID: 0635E2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. Equipo Mรฉdico
Product Type (English)
I. Equipo Mรฉdico
Trade Name (Spanish)
DIGITAL ULTRA FLOWMETER
Trade Name (English)
DIGITAL ULTRA FLOWMETER
Registration Information
Analysis ID
0635E2024 SSA
Registration Date
March 05, 2024
Manufacturer / Fabricante
Name (Spanish)
VAMASA, S.A. DE C.V.
Name (English)
VAMASA, S.A. DE C.V.