BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS)
Mexico·Clase III·II. Protesis,
órtesis y ayudas
funcionales·EMERGO S. DE R.L. DE C.V.·Registered March 07, 2024- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. Protesis, órtesis y ayudas funcionales
- Product Type (English)
- II. Protesis, órtesis y ayudas funcionales
- Trade Name (Spanish)
- PLIAFX®
- Trade Name (English)
- PLIAFX®
- Analysis ID
- 0663C2024 SSA
- Registration Date
- March 07, 2024
- 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 BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS) (BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS)) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0663C2024 SSA and manufactured by EMERGO S. DE R.L. DE C.V.. The device was registered on March 07, 2024.
This page provides complete registration details including product type (II. Protesis, órtesis y ayudas funcionales), 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.