5a8e839aa93707f426489b4e819e7b6e

MATERIAL DE OSTEOSÍNTESIS DE MAXILOFACIAL KLS MARTIN

MAXILLOFACIAL OSTEOSYNTHESIS MATERIAL KLS MARTIN
QUIRURGICOS LTDA.·IIb·Colombia INVIMA·Expires December 21, 2031
Device classification
Risk class / Clase de Riesgo
IIb
Product type (Spanish)
MEDICO QUIRURGICOS
Product type (English)
SURGICAL DOCTOR
Registration information
Analysis ID
5a8e839aa93707f426489b4e819e7b6e
Expire date
December 21, 2031
Authorized company / Fabricante
Name (Spanish)
QUIRURGICOS LTDA.
Name (English)
QUIRURGICOS LTDA.
Product use / Uso del Producto
Spanish

TODOS LOS IMPLANTES DE OSTEOSÍNTESIS ESTAN DESTINADOS A SER UTILIZADOS PARA PROCEDIMIENTRS QUIRÚRGICOS QUE REQUIEREN FIJACIÓN INTERNA POR MEDIO DE PLACAS Y TORNILLOS PARA LA ALINEACIÓN, RECONSTRUCCIÓN Y ESTABILIZACIÓN DEL TEJIDO ÓSEO. EL CRIUJANO_x000D_ RESPONSABLE DEBE ELEGIR EL TIPO Y EL TAMAÑO ADECUADO DEL IMPLANTE ESTE DE ACUERDO CON LOS REQUISITOS ANATÓMICOS Y FUNCIONES DEL PACIENTE

English

ALL OSTEOSYNTHESIS IMPLANTS ARE INTENDED TO BE USED FOR SURGICAL PROCEDURES THAT REQUIRE INTERNAL FIXATION BY MEANS OF PLATES AND SCREWS FOR THE ALIGNMENT, RECONSTRUCTION AND STABILIZATION OF BONE TISSUE. THE CRIUJANO_x000D_ RESPONSIBLE MUST CHOOSE THE APPROPRIATE TYPE AND SIZE OF THE IMPLANT THIS ACCORDING TO THE ANATOMICAL REQUIREMENTS AND FUNCTIONS OF THE PATIENT

About this record

Access comprehensive regulatory information for MATERIAL DE OSTEOSÍNTESIS DE MAXILOFACIAL KLS MARTIN (MAXILLOFACIAL OSTEOSYNTHESIS MATERIAL KLS MARTIN) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID 5a8e839aa93707f426489b4e819e7b6e and manufactured by QUIRURGICOS LTDA.. The device was registered on December 21, 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.