DURAFIBER AG.
Mexico·Clase II·V. SURGICAL AND HEALING MATERIALS·SMITH & NEPHEW, S.A. DE C.V.·Registered October 30, 2018APÓSITO ANTIMICROBIANO DESTINADO A PROPORCIONAR UN AMBIENTE HÚMEDO PARA LA HERIDA, PARA SU USO EN EL TRATAMIENTO DE HERIDAS DE ESPESOR PARCIAL Y TOTAL, INCLUIDAS LAS QUEMADURAS DE PRIMER Y SEGUNDO GRADO. PARA SER UTILIZADO UNA SOLA VEZ. NO UTILIZAR EN PAC
ANTIMICROBIAL DRESSING INTENDED TO PROVIDE A MOIST ENVIRONMENT FOR THE WOUND, FOR USE IN THE TREATMENT OF PARTIAL AND FULL THICKNESS WOUNDS, INCLUDING FIRST AND SECOND DEGREE BURNS. TO BE USED ONLY ONCE. DO NOT USE IN PAC
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- APÓSITO ANTIMICROBIANO ABSORBENTE DE FIBRAS DE CELULOSA Y ETILSULFONATO.
- Trade Name (English)
- ABSORBENT ANTIMICROBIAL DRESSING OF CELLULOSE FIBERS AND ETHYLSULFONATE.
- Analysis ID
- 2512C2018 SSA
- Registration Date
- October 30, 2018
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for DURAFIBER AG. (DURAFIBER AG.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2512C2018 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on October 30, 2018.
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.