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.
PARA TERAPIA CON ONDA DE CHOQUE EXTRACORPรREA, SE PUEDE USAR PARA DISFUNCIรN ERรCTIL (ED)
FOR EXTRACORPOREAL SHOCKWAVE THERAPY, IT CAN BE USED FOR ERECTILE DYSFUNCTION (ED)

