ANCLAJE DE SUTURA PARA HOMBRO
Mexico·Clase III·II. Protesis,
órtesis y ayudas
funcionales·SMITH & NEPHEW, S.A. DE
C.V.·Registered February 12, 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)
- ANCLAJE DE SUTURA REGENESORB™ SIN NUDOS HEALICOIL
- Trade Name (English)
- ANCLAJE DE SUTURA REGENESORB™ SIN NUDOS HEALICOIL
- Analysis ID
- 0492C2024 SSA
- Registration Date
- February 12, 2024
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for ANCLAJE DE SUTURA PARA HOMBRO (ANCLAJE DE SUTURA PARA HOMBRO) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0492C2024 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on February 12, 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.