Pure Global

Electrocardiograph - Argentina Medical Device Registration

Access comprehensive regulatory information for Electrocardiograph in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Modification medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on March 20, 2024.

This page provides complete registration details including product code (1073-220), brand name (PER NIHON), 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.

Free Database
Powered by Pure Global AI
Argentina ANMAT Data
Bilingual (Spanish/English)
Class I-II Registration Modification
Electrocardiograph
Electrocardiรณgrafo
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

ECG-3250, ECG-3350

Device Classification
Registration Type
Class I-II Registration Modification
Modificaciรณn de Registro Clase I-II
Product Code
1073-220
Brand Name
PER NIHON
NIHON KOHDEN
Product Name
Electrocardiograph
Electrocardiรณgrafo
Registration Information
Registration Date
March 20, 2024
Database ID
cmhayu26e0h6cekuzpwf2nl5q
Authorized Representative