b6a3c418d56b444123f2c88180a3d447

NIPRO HEMODIALYZER SUREFLUX- HEMODIALIZADOR NIPRO SUREFLUX

NIPRO MEDICAL CORPORATION·IIb·Colombia INVIMA·Expires October 31, 2033

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 (Spanish): NIPRO MEDICAL CORPORATION
Name (English): NIPRO MEDICAL CORPORATION

Product use / Uso del Producto

Spanish

DIAIZADORES INDICADOS PARA LOS PACIENTES QUE TENGAN UNA INSUFICIENCIA RENAL CRÓNICO O AGUDO, CUANDO LAS DIÁLISIS ESTÁN RECETADAS POR EL MÉDICO.

English

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

About this record

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.