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SISTEMA DE FIJACION DE COLUMNA Y SU INSTRUMENTAL ASOCIADO - INVIMA Registration a20d2f6ce1a680bc3a198cd4c86a64a4

Access comprehensive regulatory information for SISTEMA DE FIJACION DE COLUMNA Y SU INSTRUMENTAL ASOCIADO (COLUMN FIXATION SYSTEM AND ITS ASSOCIATED INSTRUMENTS ) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID a20d2f6ce1a680bc3a198cd4c86a64a4 and manufactured by LH S.A.S.. The device was registered on September 05, 2033.

This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
IIb
a20d2f6ce1a680bc3a198cd4c86a64a4
SISTEMA DE FIJACION DE COLUMNA Y SU INSTRUMENTAL ASOCIADO
INVIMA Analysis ID: a20d2f6ce1a680bc3a198cd4c86a64a4
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Product Use / Uso del Producto
Spanish

EL SISTEMA DE IMPLANTE DE COLUMNA NORMMED ESTÁ DISEÑADO PARA PROPORCIONAR LA MEJOR ADAPTACIÓN POSIBLE A LAS VARIACIONES ANATÓMICAS DE LOS PACIENTES. DESARROLLADO CON EL PROPÓSITO DE CORREGIR Y ESTABILIZAR LA COLUMNA. EL SISTEMA DE IMPLANTE VERTEBRAL NORMALIZADO CONSTA DE SERIES DE TORNILLOS, GANCHOS PLANOS Y PEDICULARES, VARILLAS, CAJETINES Y PLACAS DE VARIAS LONGITUDES Y TAMAÑOS. TAMBIÉN SE PUEDE PROPORCIONAR UNA VARILLA TRANSVERSAL CON CONECTORES PARA PROPORCIONAR LA MÁXIMA RIGIDEZ CUANDO SE IMPLANTA POSTERIORMENTE. LOS IMPLANTES EN EL SISTEMA ESPINAL NORMALIZADO ESTÁN INDICADOS PARA PACIENTES QUE PRESENTAN LAS SIGUIENTES PATOLOGÍAS EN LA REGIÓN TORÁCICA Y LUMBAR. _x000D_ O ESPONDILOLISTESIS_x000D_ O ENFERMEDAD DEGENERATIVA DEL DISCO_x000D_ O FRACTURAS DEL SEGMENTO ESPINAL_x000D_ O TUMOR_x000D_ O FRACTURA Y LUXACIÓN_x000D_ O ESTENOSIS_x000D_ O DESVIACIÓN DE LA COLUMNA (ESCOLIOSIS, CIFOSIS, LORDOSIS)_x000D_ O ENFERMEDAD DE SCHEUERMANN_x000D_ O PSEUDOARTROSIS_x000D_ O FUSIÓN FALLIDA_x000D_

English

THE NORMMED SPINE IMPLANT SYSTEM IS DESIGNED TO PROVIDE THE BEST POSSIBLE ADAPTATION TO PATIENTS' ANATOMICAL VARIATIONS. DEVELOPED FOR THE PURPOSE OF CORRECTING AND STABILIZING THE SPINE. THE STANDARD SPINAL IMPLANT SYSTEM CONSISTS OF SERIES OF SCREWS, FLAT AND PEDICLE HOOKS, RODS, BOXES AND PLATES OF VARIOUS LENGTHS AND SIZES. A CROSS ROD WITH CONNECTORS CAN ALSO BE PROVIDED TO PROVIDE MAXIMUM RIGIDITY WHEN IMPLANTED SUBSEQUENTLY. IMPLANTS IN THE NORMALIZED SPINAL SYSTEM ARE INDICATED FOR PATIENTS WITH THE FOLLOWING PATHOLOGIES IN THE THORACIC AND LUMBAR REGION. _x000D_ Or ESPONDILOLISTESIS_x000D_ OR DEGENERATIVE DISEASE OF THE DISCO_x000D_ OR FRACTURES OF THE ESPINAL_x000D_ SEGMENT Or TUMOR_x000D_ OR FRACTURE AND LUXACIÓN_x000D_ Or ESTENOSIS_x000D_ OR SPINAL DEVIATION (SCOLIOSIS, KYPHOSIS, LORDOSIS)_x000D_ OR SCHEUERMANN_x000D_'S DISEASE Or PSEUDOARTROSIS_x000D_ OR MERGER FALLIDA_x000D_

Device Classification
Risk Class / Clase de Riesgo
IIb
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
a20d2f6ce1a680bc3a198cd4c86a64a4
Expire Date
September 05, 2033
Authorized Company / Fabricante
Name (Spanish)
LH S.A.S.
Name (English)
LH S.A.S.