Pure Global

AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test - Argentina Medical Device Registration

Access comprehensive regulatory information for AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test in the Argentina medical device market through Pure Global AI's free database. This IVD Registration Group A and B medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on January 19, 2024.

This page provides complete registration details including product code (1716-246), brand name (AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test), 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)
IVD Registration Group A and B
AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test ISIC-525

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
1716-246
Brand Name
AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test
Product Name
AXINEA SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test
Registration Information
Registration Date
January 19, 2024
Database ID
cmhaytt5j09d4ekuz39m35tnx
Authorized Representative