1- SARS-CoV-2 Antigen Rapid Test (Swab) 2- COVID-19 Antigen Rapid Test (Oral Fluid) 3- COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) - Argentina Medical Device Registration

Access comprehensive regulatory information for 1- SARS-CoV-2 Antigen Rapid Test (Swab) 2- COVID-19 Antigen Rapid Test (Oral Fluid) 3- COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) in the Argentina medical device market through Pure Global AI's free database. This IVD Modification 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 March 25, 2024.

This page provides complete registration details including product code (2123-42), brand name (1- SARS-CoV-2 Antigen Rapid Test (Swab) 2- COVID-19 Antigen Rapid Test (Oral Fluid) 3- COVID-19 Antigen Rapid Test (Nasopharyngeal Swab)), 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.