INSTRUMENTAL PARA SISTEMA DE FIJACIÓN ESPINAL VIRAGE® OCT
Mexico·Clase I·I. MEDICAL EQUIPMENT·BIOMET MÉXICO, S.A. DE C.V.·Registered May 22, 2019EL INSTRUMENTAL PARA SISTEMA DE FIJACIÓN ESPINAL VIRAGE® OCT ESTÁ INDICADO PARA IMPLANTAR DISPOSITIVOS QUE PROMUEVEN LA FUSIÓN DE LA COLUMNA OCCIPITO-CERVICAL, CERVICAL Y TORÁCICA (OCCIPUCIO- T3) EN PACIENTES CON: ENFERMEDAD DEGENERATIVA DE DISCO (DDD);
THE VIRAGE® OCT SPINAL FIXATION SYSTEM INSTRUMENTS ARE INDICATED FOR IMPLANTING DEVICES THAT PROMOTE FUSION OF THE OCCIPITO-CERVICAL, CERVICAL AND THORACIC SPINE (OCCIPUT-T3) IN PATIENTS WITH: DEGENERATIVE DISC DISEASE (DDD);
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- INSTRUMENTAL QUIRÚRGICO ORTOPÉDICO MANUAL.
- Trade Name (English)
- MANUAL ORTHOPEDIC SURGICAL INSTRUMENTS.
- Analysis ID
- 1119E2019 SSA
- Registration Date
- May 22, 2019
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for INSTRUMENTAL PARA SISTEMA DE FIJACIÓN ESPINAL VIRAGE® OCT (INSTRUMENTS FOR SPINAL FIXATION SYSTEM VIRAGE® OCT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1119E2019 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on May 22, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.