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RELLENO DÉRMICO INYECTABLE - COFEPRIS Registration 1316C2022 SSA

Access comprehensive regulatory information for RELLENO DÉRMICO INYECTABLE (RELLENO DÉRMICO INYECTABLE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1316C2022 SSA and manufactured by EMERGO, S. DE R.L. DE C.V.. The device was registered on November 04, 2022.

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 III
1316C2022 SSA
RELLENO DÉRMICO INYECTABLE
COFEPRIS Analysis ID: 1316C2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. Materiales quirúrgicos y de curación
Product Type (English)
V. Materiales quirúrgicos y de curación
Trade Name (Spanish)
NEURAMIS® LIDOCAINE
Trade Name (English)
NEURAMIS® LIDOCAINE
Registration Information
Analysis ID
1316C2022 SSA
Registration Date
November 04, 2022
Manufacturer / Fabricante
Name (English)
EMERGO, S. DE R.L. DE C.V.