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ECMO Extracorporeal Membrane Oxygenation System - Argentina Medical Device Registration

Access comprehensive regulatory information for ECMO Extracorporeal Membrane Oxygenation System in the Argentina medical device market through Pure Global AI's free database. This Registration Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 03, 2024.

This page provides complete registration details including product code (251-118), brand name (MC3), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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Argentina ANMAT Data
Bilingual (Spanish/English)
Registration Class III-IV
ECMO Extracorporeal Membrane Oxygenation System
Sistema de oxigenación por membrana extracorpórea ECMO
Argentina Medical Device Registration
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Product Information

48145 Nautilus TM ECMO Oxygenator 48145E Nautilus TM ECMO Oxygenator 48135 Nautilus TM Smart ECMO Module 48135E Nautilus TM Smart ECMO Module

Spanish:

48145 Nautilus TM Oxigenador ECMO 48145E Nautilus TM Oxigenador ECMO 48135 Nautilus TM Smart Módulo ECMO 48135E Nautilus TM Smart Módulo ECMO

Device Classification
Registration Type
Registration Class III-IV
Registro Clase III-IV
Product Code
251-118
Brand Name
MC3
Product Name
ECMO Extracorporeal Membrane Oxygenation System
Sistema de oxigenación por membrana extracorpórea ECMO
Registration Information
Registration Date
June 03, 2024
Database ID
cmhaytsdm08ojekuztye84915
Documents
Authorized Representative