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DORNIER ARIES - COFEPRIS Registration 309E2019 SSA

Access comprehensive regulatory information for DORNIER ARIES (DORNIER ARIES) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 309E2019 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on February 18, 2019.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 III
309E2019 SSA
DORNIER ARIES
COFEPRIS Analysis ID: 309E2019 SSA
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Product Use / Uso del Producto
Spanish

PARA TERAPIA CON ONDA DE CHOQUE EXTRACORPร“REA, SE PUEDE USAR PARA DISFUNCIร“N ERร‰CTIL (ED)

English

FOR EXTRACORPOREAL SHOCKWAVE THERAPY, IT CAN BE USED FOR ERECTILE DYSFUNCTION (ED)

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
Emisor de ondas de choque electromagnรฉticas
Trade Name (English)
Electromagnetic shock wave emitter
Registration Information
Analysis ID
309E2019 SSA
Registration Date
February 18, 2019
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL, S.A. DE C.V.