MEDILAS H UROPULSE - COFEPRIS Registration 1796E2018 SSA
Access comprehensive regulatory information for MEDILAS H UROPULSE (MEDILAS H UROPULSE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1796E2018 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on July 24, 2018.
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 UTILIZARSE EN EL CORTE, VAPORIZACIÓN, ABLACIÓN Y COAGULACIÓN DEL TEJIDO BLANDO EN CONJUNTO CON EL EQUIPO ENDOSCÓPICO O PARA LA CIRUGÍA ABIERTA PARA LA CIRUGÍA DE CONTACTO Y DE NO CONTACTO CON O SIN PIEZA MANUAL PARA USARSE EN LA INCISIÓN Y ESCISIÓN,
FOR USE IN CUTTING, VAPORIZING, ABLATION AND COAGULATION OF SOFT TISSUE IN CONJUNCTION WITH ENDOSCOPIC EQUIPMENT OR FOR OPEN SURGERY FOR CONTACT AND NON-CONTACT SURGERY WITH OR WITHOUT A HANDPIECE FOR USE IN INCISION AND EXCISION,