Mexico COFEPRIS registration 0635E2024 SSA
FLUJOMETRO
EN: FLUJOMETRO
Mexico·Clase II·I. Equipo Médico·VAMASA, S.A. DE C.V.·Registered March 05, 2024Device classification
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. Equipo Médico
- Product Type (English)
- I. Equipo Médico
- 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.
About this record
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 Médico), 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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