STRAUMANN® MAXRESORB® INJECT - COFEPRIS Registration 1324C2018 SSA
Access comprehensive regulatory information for STRAUMANN® MAXRESORB® INJECT (STRAUMANN® MAXRESORB® INJECT) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1324C2018 SSA and manufactured by MANOHAY MÉXICO, S.A DE C.V.. The device was registered on June 04, 2018.
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.
ES UN SUSTITUTO ÓSEO SINTÉTICO Y OSTEOCONDUCTOR QUE SE APLICA EN FORMA DE PASTA Y ESTÁ DESTINADO A SER UTILIZADO COMO UN ANDAMIO PARA SOPORTAR EL CRECIMIENTO INTERNO DEL HUESO VIABLE ADYACENTE EN DEFECTOS QUE NO SON INTRÍNSECOS A LA ESTABILIDAD DE LA ESTR
IT IS A SYNTHETIC BONE SUBSTITUTE AND OSTEOCONDUCTOR THAT IS APPLIED IN PASTE FORM AND IS INTENDED TO BE USED AS A SCAFFOLD TO SUPPORT THE INTERNAL GROWTH OF ADJACENT VIABLE BONE IN DEFECTS THAT ARE NOT INTRINSIC TO THE STABILITY OF THE ESTR.