IM-CURE KIT - COFEPRIS Registration 1415E2021 SSA
Access comprehensive regulatory information for IM-CURE KIT (IM-CURE KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1415E2021 SSA and manufactured by HIOSSEN DE MÉXICO,S.A. DE C.V.. The device was registered on September 15, 2021.
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.
EL IM-CURE KIT ESTÁ COMPUESTO PORHERRAMIENTAS UTILIZADAS PARACONTROLAR LA ENFERMEDADPERIIMPLANTARIAELIMINANDOLASCAUSASDELAINFLAMACIÓN,INCLUYENDOLAPLACA,ELSARROYLOSCUERPOSEXTRAÑOSDELASUPERFICIE DE UN IMPLANTE.
THE IM-CURE KIT CONSISTS OF TOOLS USED TO CONTROL PERI-IMPLANT DISEASE BY ELIMINATING THE CAUSES OF INFLAMMATION, INCLUDING LAPLACA, SLOUCH AND FOREIGN BODIES FROM THE SURFACE OF AN IMPLANT.