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NIPRO HEMODIALYZER / NIPRO HEMODIALIZADOR - INVIMA Registration 3668cd17cd8190faa37ab1ba8df129eb

Access comprehensive regulatory information for NIPRO HEMODIALYZER / NIPRO HEMODIALIZADOR (NIPRO HEMODIALYZER / NIPRO HEMODIALIZADOR ) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID 3668cd17cd8190faa37ab1ba8df129eb and manufactured by NIPRO MEDICAL CORPORATION. The device was registered on October 31, 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
3668cd17cd8190faa37ab1ba8df129eb
NIPRO HEMODIALYZER / NIPRO HEMODIALIZADOR
INVIMA Analysis ID: 3668cd17cd8190faa37ab1ba8df129eb
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Product Use / Uso del Producto
Spanish

DIAIZADORES INDICADOS PARA LOS PACIENTES QUE TENGAN UNA INSUFICIENCIA RENAL CRร“NICO O AGUDO, CUANDO LAS DIALISIS ESTAN RECETADAS POR EL Mร‰DICO.

English

DIAIZERS INDICATED FOR PATIENTS WHO HAVE CHRONIC OR ACUTE RENAL FAILURE, WHEN DIALYSIS IS PRESCRIBED BY THE DOCTOR.

Device Classification
Risk Class / Clase de Riesgo
IIb
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
3668cd17cd8190faa37ab1ba8df129eb
Expire Date
October 31, 2033
Authorized Company / Fabricante
Name (English)
NIPRO MEDICAL CORPORATION