Mexico COFEPRIS registration 1056C2024 SSA

DIALIZADOR DE FIBRA HUECA.

EN: DIALIZADOR DE FIBRA HUECA.
Mexico flagMexico·Clase II·V. Materiales quirúrgicos y de curación·EMERGO, S. DE R.L. DE C.V.·Registered April 15, 2024
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)
WEGO HOLLOW FIBER DIALYZER.
Trade Name (English)
WEGO HOLLOW FIBER DIALYZER.
Registration information
Analysis ID
1056C2024 SSA
Registration Date
April 15, 2024
Manufacturer / Fabricante
Name (English)
EMERGO, S. DE R.L. DE C.V.
About this record

Access comprehensive regulatory information for DIALIZADOR DE FIBRA HUECA. (DIALIZADOR DE FIBRA HUECA.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1056C2024 SSA and manufactured by EMERGO, S. DE R.L. DE C.V.. The device was registered on April 15, 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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