Mexico COFEPRIS registration 0148E2024 SSA
LÁSER DE DIODO.
EN: LÁSER DE DIODO.
Mexico·Clase II·I. Equipo Médico·VAMASA, S.A. DE C.V.·Registered January 17, 2024Device classification
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. Equipo Médico
- Product Type (English)
- I. Equipo Médico
- Trade Name (Spanish)
- GEMINI EVO 810 + 980.
- Trade Name (English)
- GEMINI EVO 810 + 980.
Registration information
- Analysis ID
- 0148E2024 SSA
- Registration Date
- January 17, 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 LÁSER DE DIODO. (LÁSER DE DIODO.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0148E2024 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on January 17, 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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