TEGADERM SILICONE FOAM - COFEPRIS Registration 1663C2020 SSA
Access comprehensive regulatory information for TEGADERM SILICONE FOAM (TEGADERM SILICONE FOAM) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1663C2020 SSA and manufactured by 3M MÉXICO, S.A. DE C.V.. The device was registered on December 16, 2020.
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 ESTÁ DISEÑADO PARA ELTRATAMIENTO DE HERIDAS DE ESPESORPARCIALYTOTALCONEXUDADOBAJOAALTO,COMO ÚLCERAS POR PRESIÓN, ÚLCERASVENOSAS EN LAS PIERNAS, ÚLCERASNEUROPÁTICAS, ÚLCERAS ARTERIALES,DESGARROS CUTÁNEOS, HERIDASQUIRÚRGICAS, QUEMADURAS SUPERFICIALESDE ESPESOR PARCIAL Y ZONAS DONANTES
THE DRESSING IS DESIGNED FOR THE TREATMENT OF PARTIAL AND TOTAL THICKNESS WOUNDS WITH LOW TO HIGH DISCOURAGEMENT, SUCH AS PRESSURE ULCERS, VENOUS LEG ULCERS, NEUROPATHIC ULCERS, ARTERIAL ULCERS, SKIN TEARS, SURGICAL WOUNDS, PARTIAL THICKNESS SUPERFICIAL BURNS AND DONOR AREAS