RELLENO DÉRMICO INYECTABLE
Mexico·Clase III·V. Materiales quirúrgicos y
de curación·EMERGO, S. DE R.L.
DE C.V.·Registered November 04, 2022- 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
- Analysis ID
- 1316C2022 SSA
- Registration Date
- November 04, 2022
- Name (Spanish)
- EMERGO, S. DE R.L. DE C.V.
- Name (English)
- EMERGO, S. DE R.L. DE C.V.
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.