MS SA IMPLANT - COFEPRIS Registration 986C2021 SSA
Access comprehensive regulatory information for MS SA IMPLANT (MS SA IMPLANT) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 986C2021 SSA and manufactured by HIOSSEN DE MÉXICO,S.A. DE C.V.. The device was registered on October 06, 2021.
This page provides complete registration details including product type (IV. DENTAL SUPPLIES), 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.
MS SA IMPLANT ES UNA RAÍZ DENTALARTIFICIAL PARA RESTAURACIONESDENTALESDEFECTUOSAS,YESTÁDISEÑADOPARASERUTILIZADOENELPROCEDIMIENTODE IMPLANTE DENTAL. SE INSERTAQUIRÚRGICAMENTEENELHUESOALVEOLARMAXILAR O SUBMAXILAR, Y REEMPLAZA LARAÍZDEUNDIENTENATURAL.ELIMPLANTEMSSAUNIFICAELCUERPOYELPILARDELAPRÓTESIS DE FORMA QUE SE PUEDARESOLVERLAFUERZADELAMORDIDA.ESUNIMPLANTE DE TIPO NO SUMERGIDOADECUADO PARA PACIENTES QUEPRESENTAN CRESTAS ESTRECHAS.
MS SA IMPLANT IS AN ARTIFICIAL TOOTH ROOT FOR DEFECTIVE DENTAL RESTORATIONS, AND IS DESIGNED TO BE USED IN THE DENTAL IMPLANT PROCEDURE. IT IS SURGICALLY INSERTED INTO THE ALVEOLARMAXILLARY OR SUBMAXILLARY BONE, AND REPLACES NATURAL LARAÍZDEUNDIENTE. THE IMPLANT UNIFIES THE BODY AND THE PILLAR OF THE PROSTHESIS SO THAT THE FORCE OF THE MUZZLED CAN BE RESOLVED. A NON-SUBMERGED TYPE IMPLANT SUITABLE FOR PATIENTS WITH NARROW RIDGES.