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SISTEMA DE PRÓTESIS DE RODILLA - INVIMA Registration ae6fd8b27871e997705157665e0419a6

Access comprehensive regulatory information for SISTEMA DE PRÓTESIS DE RODILLA (KNEE PROSTHESIS SYSTEM) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID ae6fd8b27871e997705157665e0419a6 and manufactured by MADHOS S.A.S. The device was registered on February 16, 2031.

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
ae6fd8b27871e997705157665e0419a6
SISTEMA DE PRÓTESIS DE RODILLA
INVIMA Analysis ID: ae6fd8b27871e997705157665e0419a6
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Product Use / Uso del Producto
Spanish

"INDICADA PARA EL TRATAMIENTO QUIRÚRGICO DE: *ARTRITIS DEGENERATIVA. • ARTRITIS REUMATOIDE. • ARTRITIS POSTRAUMÁTICA. • UNA ARTICULACIÓN SEVERAMENTE DOLOROSA Y/O SEVERAMENTE DISCAPACITADA COMO RESULTADO DE OTRA ARTRITIS NO INFLAMATORIA. • DEFORMIDADES MODERADAS EN VALGO, VARO O FLEXIÓN EN LAS CUALES LAS ESTRUCTURAS LIGAMENTOSAS PUEDEN REGRESAR A SU FUNCIÓN Y ESTABILIDAD ADECUADAS. • OSTEONECROSIS DE LA RODILLA EN LA MAYOR PARTE DE LA SUPERFICIE ÓSEA U OTRA ENFERMEDAD QUE NO PUEDE TRATARSE CON OTROS MÉTODOS QUIRÚRGICOS. • UN IMPLANTE ANTERIOR FALLIDO." _x000D_ _x000D_ _x000D_

English

"INDICATED FOR THE SURGICAL TREATMENT OF: *DEGENERATIVE ARTHRITIS. •RHEUMATOID ARTHRITIS. • POSTTRAUMATIC ARTHRITIS. • A SEVERELY PAINFUL AND/OR SEVERELY DISABLED JOINT AS A RESULT OF OTHER NON-INFLAMMATORY ARTHRITIS. • MODERATE VALGUS, VARUS OR FLEXION DEFORMITIES IN WHICH LIGAMENTOUS STRUCTURES CAN RETURN TO THEIR PROPER FUNCTION AND STABILITY. • OSTEONECROSIS OF THE KNEE ON MOST OF THE BONE SURFACE OR ANOTHER DISEASE THAT CANNOT BE TREATED WITH OTHER SURGICAL METHODS. • A FAILED PREVIOUS IMPLANT." _x000D_ _x000D_ _x000D_

Device Classification
Risk Class / Clase de Riesgo
IIb
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
ae6fd8b27871e997705157665e0419a6
Expire Date
February 16, 2031
Authorized Company / Fabricante
Name (Spanish)
MADHOS S.A.S
Name (English)
MADHOS S.A.S