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Sars-CoV-2 & RSV & Influenza A+B Antigen Combo Rapid Test - Argentina Medical Device Registration

Access comprehensive regulatory information for Sars-CoV-2 & RSV & 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 August 14, 2024.

This page provides complete registration details including product code (2123-116), brand name (Sars-CoV-2 & RSV & 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.

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Argentina ANMAT Data
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IVD Registration Group A and B
Sars-CoV-2 & RSV & Influenza A+B Antigen Combo Rapid Test
Argentina Medical Device Registration
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Product Information

Sars-CoV-2 & RSV & Influenza A+B Antigen Combo Rapid Test

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
2123-116
Brand Name
Sars-CoV-2 & RSV & Influenza A+B Antigen Combo Rapid Test
Product Name
Sars-CoV-2 & RSV & Influenza A+B Antigen Combo Rapid Test
Registration Information
Registration Date
August 14, 2024
Database ID
cmhaytq4a077jekuzoo8hrshu
Authorized Representative