2123-421- 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 · 1- SARS-CoV-2 Antigen Rapid Test (Swab) 2- COVID-19 Antigen Rapid Test (Oral Fluid) 3- COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) · LABORATORIOS JAYOR S.R.L. · Registered March 25, 2024
IVD Modification Group A and B- Registration Type
- IVD Modification Group A and B
- Modificación IVD Grupo A y B
- 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)
- Product 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)
- Registration Date
- March 25, 2024
- Database ID
- cmhayu26e0h4nekuz7fh4p2eb
1- ISCO-ACO502 2- INCP-ACO802 3- INCP-ACO502
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.