DORNIER ARIES
Mexico·Clase III·I. MEDICAL EQUIPMENT·LEVBETH MEDICAL, S.A. DE C.V.·Registered February 18, 2019PARA TERAPIA CON ONDA DE CHOQUE EXTRACORPÓREA, SE PUEDE USAR PARA DISFUNCIÓN ERÉCTIL (ED)
FOR EXTRACORPOREAL SHOCKWAVE THERAPY, IT CAN BE USED FOR ERECTILE DYSFUNCTION (ED)
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- Emisor de ondas de choque electromagnéticas
- Trade Name (English)
- Electromagnetic shock wave emitter
- Analysis ID
- 309E2019 SSA
- Registration Date
- February 18, 2019
- Name (Spanish)
- LEVBETH MEDICAL, S.A. DE C.V.
- Name (English)
- LEVBETH MEDICAL, S.A. DE C.V.
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.