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TUBO ENDOTRAQUEAL. - COFEPRIS Registration 0959C2024 SSA

Access comprehensive regulatory information for TUBO ENDOTRAQUEAL. (TUBO ENDOTRAQUEAL.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0959C2024 SSA and manufactured by EMERGO, S. DE R.L. DE C.V.. The device was registered on April 05, 2024.

This page provides complete registration details including product type (V. Materiales quirúrgicos y de curación), 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.

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COFEPRIS Official Data
Clase II
0959C2024 SSA
TUBO ENDOTRAQUEAL.
COFEPRIS Analysis ID: 0959C2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
V. Materiales quirúrgicos y de curación
Product Type (English)
V. Materiales quirúrgicos y de curación
Trade Name (Spanish)
MICROCUFF* ENDOTRACHEAL TUBE
Trade Name (English)
MICROCUFF* ENDOTRACHEAL TUBE
Registration Information
Analysis ID
0959C2024 SSA
Registration Date
April 05, 2024
Manufacturer / Fabricante
Name (English)
EMERGO, S. DE R.L. DE C.V.