VENDA DE FIBRA DE VIDRIO. NO ESTÉRIL. MEDLINE® - COFEPRIS Registration 1993C2019 SSA

Access comprehensive regulatory information for VENDA DE FIBRA DE VIDRIO. NO ESTÉRIL. MEDLINE® (FIBERGLASS BANDAGE. NOT STERILE. MEDLINE®) in the Mexico medical device market through Pure Global AI's free database. This Clase I-Bajo Riesgo medical device is registered under COFEPRIS analysis ID 1993C2019 SSA and manufactured by MEDLINE MÉXICO, S. DE R.L. DE C.V.. The device was registered on October 16, 2019.

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.