HEALICOIL™ REGENESORB
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·SMITH & NEPHEW, S.A. DE C.V.·Registered January 04, 2018LOS ANCLAJES PARA SUTURAS HEALICOIL REGENESORB ESTÁN DISEÑADOS PARA LA RECONEXIÓN DE TEJIDO BLANDO AL HUESO EN HOMBRO, CODO, RODILLA, PIE Y TOBILLO.
HEALICOIL REGENESORB SUTURE ANCHORS ARE DESIGNED FOR SOFT TISSUE RECONNECTION TO BONE IN SHOULDER, ELBOW, KNEE, FOOT AND ANKLE.
- 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)
- ANCLAJE PARA SUTURA TIPO SACA CORCHO BIOCOMPUESTO Y BIOABSORBIBLE (BIODEGRADABLE)
- Trade Name (English)
- ANCHOR FOR BIOCOMPOSITE AND BIOABSORBABLE CORK SUTURE TYPE (BIODEGRADABLE)
- Analysis ID
- 76C2018 SSA
- Registration Date
- January 04, 2018
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for HEALICOIL™ REGENESORB (HEALICOIL™ REGENESORB) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 76C2018 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on January 04, 2018.
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.