NIPRO Medical Corporation - Authorized Company Profile

Explore comprehensive authorized company profile for NIPRO Medical Corporation through Pure Global AI's free Argentina medical device database. This company manufactures 133 medical devices registered with ANMAT across 11 registration types. Their registration history spans from Nov 30, 2017 to Jul 19, 2024.

This page provides detailed insights including recent registrations, registration type distribution (Class I-II Registration: 22, Revalidation of Registration I-II-III-IV: 53, Registration Class III-IV: 15, and more), and complete regulatory information from the official Argentina ANMAT (National Administration of Drugs, Foods and Medical Technology) medical device database with bilingual Spanish/English support. Pure Global AI offers free access to Argentina's complete medical device registry.

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133 Devices

11 Registration Types

NIPRO Medical Corporation

Authorized Company

133

Total Devices

11

Registration Types

2017

Earliest

2024

Latest

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Recent Registrations

Latest 20 ANMAT device registrations

Continuous glucose monitoring system.

Sistema de monitorización continua de glucosa.

877-201

Registration Class III-IV

Infusion set

Set de infusión

877-132

Class I-II Registration Modification

Perfusion System

Sistema de Perfusión

877-200

Registration Class III-IV

Cardiopledic System

Sistema de Cardioplegía

877-85

Revalidation of Registration I-II-III-IV

Synthetic Hemodialyzer

Hemodializador Sintético

877-91

Revalidation of Registration I-II-III-IV

Synthetic Hemodialyzer

Hemodializador Sintético

877-123

Revalidation of Registration I-II-III-IV

Safetouch Pericranial Needle Equipment

Equipo de Agujas Pericraneales Safetouch

877-90

Revalidation of Registration I-II-III-IV

Synthetic Hemodialyzer

Hemodializador Sintético

877-122

Revalidation of Registration I-II-III-IV

Infusion Pump for insulin.

Bomba de Infusión para insulina.

877-202

Registration Class III-IV

Spinal needle

Aguja espinal

877-3

Revalidation of Registration I-II-III-IV

Guidewire Extension Catheter

Catéter de Extensión de Guía

877-203

Registration Class III-IV

Synthetic hollow fiber dialysis filter

Filtro para diálisis de fibra hueca sintético

877-91

Registration modification (non-agile) Class III-IV

Sodium bicarbonate for Hemodialysis.

Bicarbonato sódico para Hemodiálisis.

877-115

Revalidation of Registration I-II-III-IV

Synthetic hollow fiber dialysis filter

Filtro para diálisis de fibra hueca sintético

877-40

Revalidation of Registration I-II-III-IV

Disposable Plastic Syringe Without Needle

Jeringa de Plástico Desechable sin Aguja

877-119

Revalidation of Registration I-II-III-IV

Long-Acting Double Lumen Hemodialysis Catheters

Catéteres para Hemodiálisis Doble Lumen de Larga Duración

877-18

Revalidation of Registration I-II-III-IV

Synthetic Hemodialyzer

Hemodializador Sintético

877-92

Revalidation of Registration I-II-III-IV

Disposable Plastic Syringe with Needle.

Jeringa de Plástico Desechable con Aguja.

877-118

Revalidation of Registration I-II-III-IV

Infusion set

Set de infusión

877-132

Class I-II Registration Modification

Pericranial needles

Agujas Pericraneales

877-20

Revalidation of Registration I-II-III-IV

Registration Type Distribution

Devices by registration type

Revalidation of Registration I-II-III-IV

53

39.8% of total

Class I-II Registration

22

16.5% of total

Registration Class III-IV

15

11.3% of total

Class I-II Registration Modification

8

6.0% of total

Modification of Agile Registration Class III-IV

8

6.0% of total

Revalidation + Modification of Class I-II Registration

7

5.3% of total

Registration modification (non-agile) Class III-IV

6

4.5% of total

Class I-II Registration Revalidation

6

4.5% of total

IVD Registration Group A and B

6

4.5% of total

IVD Modification Group A and B

1

0.8% of total

Agile modification of product registration for IVD diagnostics - Group C and D

1

0.8% of total