GENTILFOAM. - COFEPRIS Registration 179C2021 SSA
Access comprehensive regulatory information for GENTILFOAM. (GENTILFOAM.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 179C2021 SSA and manufactured by PROMESURGICAL, S.A.DE C.V.. The device was registered on February 09, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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 APÓSITO GENTILFOAM ESTÁ INDICADOPARA EL TRATAMIENTO DE ÚLCERASVENOSAS, ÚLCERAS ARTERIALES, ÚLCERASPOR PRESIÓN, ÚLCERAS DIABÉTICAS,HERIDASSUTURADAS,QUEMADURASDE1ºY2ºGRADOYZONASDONANTES. GENTILFOAMSE PUEDE UTILIZAR DEBAJO DE VENDAS OMEDIAS DE COMPRESIÓN.
THE GENTILFOAM DRESSING IS INDICATED FOR THE TREATMENT OF VENOUS ULCERS, ARTERIAL ULCERS, PRESSURE ULCERS, DIABETIC ULCERS, SUTURED WOUNDS, BURNS OF 1ST AND 2ND DEGREE and donor areas. GENTILFOAMSE CAN BE USED UNDER BANDAGES COMPRESSION SOCKS.