CROSSWAY CATÉTER DEDILATACIÓN PARA ACTP
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·MEDSTENT, S.A. DE C.V.·Registered March 05, 2021POCATÉTER DE DILATACIÓN PARA ACTP
DILATION POCATHETER FOR PTCA
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- CATÉTER DE DILATACIÓN PARA ACTP
- Trade Name (English)
- DILATION CATHETER FOR PTCA
- Analysis ID
- 784C2021 SSA
- Registration Date
- March 05, 2021
- Name (Spanish)
- MEDSTENT, S.A. DE C.V.
- Name (English)
- MEDSTENT, S.A. DE C.V.
Access comprehensive regulatory information for CROSSWAY CATÉTER DEDILATACIÓN PARA ACTP (CROSSWAY DEDILATATION CATHETER FOR PTCA) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 784C2021 SSA and manufactured by MEDSTENT, S.A. DE C.V.. The device was registered on March 05, 2021.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.