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KYPHON® HV-R BONE CEMENT- CEMENTO OSEO RADIOPACO DE ALTA VISCOSIDAD - INVIMA Registration 6577ed40cadfece878a0b53e8a0aa7d0

Access comprehensive regulatory information for KYPHON® HV-R BONE CEMENT- CEMENTO OSEO RADIOPACO DE ALTA VISCOSIDAD (KYPHON® HV-R BONE CEMENT - HIGH VISCOSITY RADIOPAQUE BONE CEMENT) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 6577ed40cadfece878a0b53e8a0aa7d0 and manufactured by MEDTRONIC INC. The device was registered on September 29, 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
III
6577ed40cadfece878a0b53e8a0aa7d0
KYPHON® HV-R BONE CEMENT- CEMENTO OSEO RADIOPACO DE ALTA VISCOSIDAD
INVIMA Analysis ID: 6577ed40cadfece878a0b53e8a0aa7d0
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Product Use / Uso del Producto
Spanish

EL CEMENTO ÓSEO KYPHON® HV-R® ESTÁ INDICADO PARA USARLO COMO MATERIAL DE FIJACIÓN EN LAS FRACTURAS DE COMPRESION VERTEBRAL DURANTE EL TRATAMIENTO DE CIFOPLASTIA DONDE LA PERDIDA DE SUSTANCIA OSEA DEBIDO A LA OSTEOPOROSIS O RECALCITRANCIA DE LA FRACTURA, HACEN INEFECTIVOS LOS PROCEIDMIENTOS CONVENCIONALES; ESTA INDICADO PARA EL TRATAMIENTO DE FRACTURAS PATOLÓGICAS DE LOS CUERPOS VERTEBRALES DEBIDAS A OSTEOPOROSIS, CÁNCER O LESIONES BENIGNAS UTILIZANDO UN PROCEDIMIENTO DE CIFOPLASTIA O VERTEBROPLASTIA.

English

KYPHON® HV-R® BONE CEMENT IS INDICATED FOR USE AS A FIXATION MATERIAL IN VERTEBRAL COMPRESSION FRACTURES DURING KYPHOPLASTY TREATMENT WHERE THE LOSS OF BONE SUBSTANCE DUE TO OSTEOPOROSIS OR RECALCITRANCE OF THE FRACTURE RENDER CONVENTIONAL PROCEDURES INEFFECTIVE; IT IS INDICATED FOR THE TREATMENT OF PATHOLOGICAL FRACTURES OF THE VERTEBRAL BODIES DUE TO OSTEOPOROSIS, CANCER, OR BENIGN LESIONS USING A KYPHOPLASTY OR VERTEBROPLASTY PROCEDURE.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
6577ed40cadfece878a0b53e8a0aa7d0
Expire Date
September 29, 2033
Authorized Company / Fabricante
Name (Spanish)
MEDTRONIC INC
Name (English)
MEDTRONIC INC