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NIPRO HEMODIALYZER SUREFLUX- HEMODIALIZADOR NIPRO SUREFLUX - INVIMA Registration b6a3c418d56b444123f2c88180a3d447

Access comprehensive regulatory information for NIPRO HEMODIALYZER SUREFLUX- HEMODIALIZADOR NIPRO SUREFLUX (NIPRO HEMODIALYZER SUREFLUX- HEMODIALIZADOR NIPRO SUREFLUX) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID b6a3c418d56b444123f2c88180a3d447 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
b6a3c418d56b444123f2c88180a3d447
NIPRO HEMODIALYZER SUREFLUX- HEMODIALIZADOR NIPRO SUREFLUX
INVIMA Analysis ID: b6a3c418d56b444123f2c88180a3d447
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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 DIรLISIS ESTรN RECETADAS POR EL Mร‰DICO.

English

DIAIZERS INDICATED FOR PATIENTS WHO HAVE CHRONIC OR ACUTE KIDNEY 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
b6a3c418d56b444123f2c88180a3d447
Expire Date
October 31, 2033
Authorized Company / Fabricante
Name (English)
NIPRO MEDICAL CORPORATION