Mexico COFEPRIS registration 1546E2024 SSA

SISTEMA DE LÁSER DERMATOLÓGICO.

EN: SISTEMA DE LÁSER DERMATOLÓGICO.
Mexico flagMexico·Clase II·I. Equipo Médico·ARFAMEX, S.A. DE C.V.·Registered May 24, 2024
Device classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
FAMILIA GENTLEMAX DE SISTEMA LÁSER.
Trade Name (English)
FAMILIA GENTLEMAX DE SISTEMA LÁSER.
Registration information
Analysis ID
1546E2024 SSA
Registration Date
May 24, 2024
Manufacturer / Fabricante
Name (Spanish)
ARFAMEX, S.A. DE C.V.
Name (English)
ARFAMEX, S.A. DE C.V.
About this record

Access comprehensive regulatory information for SISTEMA DE LÁSER DERMATOLÓGICO. (SISTEMA DE LÁSER DERMATOLÓGICO.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1546E2024 SSA and manufactured by ARFAMEX, S.A. DE C.V.. The device was registered on May 24, 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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