OCLUSOR PARA CONDUCTO ARTERIOSO PERSISTENTE
- 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)
- OCCLUTECH® PDA OCCLUDER PROCEDURE PACK
- Trade Name (English)
- OCCLUTECH® PDA OCCLUDER PROCEDURE PACK
- Analysis ID
- 1191C2024 SSA
- Registration Date
- April 26, 2024
- Name (Spanish)
- MEDSTENT, S.A. DE C.V.
- Name (English)
- MEDSTENT, S.A. DE C.V.
Access comprehensive regulatory information for OCLUSOR PARA CONDUCTO ARTERIOSO PERSISTENTE (OCLUSOR PARA CONDUCTO ARTERIOSO PERSISTENTE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1191C2024 SSA and manufactured by MEDSTENT, S.A. DE C.V.. The device was registered on April 26, 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.