GENTILTAC (SOFT SILICONEINTERFACE LAYER). - COFEPRIS Registration 841C2021 SSA
Access comprehensive regulatory information for GENTILTAC (SOFT SILICONEINTERFACE LAYER). (GENTILTAC (SOFT SILICONEINTERFACE LAYER).) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 841C2021 SSA and manufactured by PROMESURGICAL, S.A.DE C.V.. The device was registered on May 13, 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.
GENTILTAC SE PUEDE UTILIZAR ENLACERACIONES, DESGARROS CUTÁNEOS,INCISIONES QUIRÚRGICAS, PARCIALES YTOTALES INJERTOS DE ESPESOR, DAÑOCUTÁNEO INDUCIDO POR RADIOTERAPIA,ÚLCERASENLASPIERNAS,ÚLCERASDELPIEDIABÉTICO, QUEMADURAS DE ESPESORPARCIAL,CUALQUIERÁREADEPIELFRÁGIL.ESTÉRIL POR ÓXIDO DE ETILENO.
GENTILTAC CAN BE USED LINKAGES, SKIN TEARS, SURGICAL INCISIONS, PARTIAL AND TOTAL THICKNESS GRAFTS, SKIN DAMAGE INDUCED BY RADIOTHERAPY, LEG ULCERS, DIABETICFOOT ULCERS, PARTIAL THICKNESS BURNS, ANY AREA OF FRAGILE SKIN. STERILE BY ETHYLENE OXIDE.