FAMILIA DE CARDIOVERSORESDESFIBRILADORES IMPLANTABLESACTICOR/RIVACOR- BIOTRONIK - COFEPRIS Registration 896C2021 SSA
Access comprehensive regulatory information for FAMILIA DE CARDIOVERSORESDESFIBRILADORES IMPLANTABLESACTICOR/RIVACOR- BIOTRONIK (FAMILY OF CARDIOVERSORESDEFIBRILLATORSIMPLANTABLE DEFIBRILLATORSACTICOR / RIVACOR- BIOTRONIK) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 896C2021 SSA and manufactured by ASESORES MÉDICOBIOLÓGICOS, S.A. DEC.V.. The device was registered on May 26, 2021.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.
ACTICOR, RIVACOR ES UNA FAMILIA DECARDIOVERSORES DESFIBRILADORESIMPLANTABLES(CONOCIDOSTAMBIÉNENLAPRÁCTICAMÉDICACOMODESFIBRILADORESAUTOMÁTICOS IMPLANTABLES DAI) CON ELOBJETIVO PRINCIPAL DE PREVENIR LAMUERTE SÚBITA CARDÍACA.
ACTICOR, RIVACOR IS A FAMILY OF IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (ALSO KNOWN IN MEDICAL PRACTICE AS ICD IMPLANTABLE CARDIOVERTER DEFIBRILLATORS) WITH THE MAIN OBJECTIVE OF PREVENTING SUDDEN CARDIAC DEATH.