Chemiluminescent, qualitative and/or quantitative immunoassay, serology, Toxoplasma and CMV - Argentina Medical Device Registration
Access comprehensive regulatory information for Chemiluminescent, qualitative and/or quantitative immunoassay, serology, Toxoplasma and CMV in the Argentina medical device market through Pure Global AI's free database. This Non-agile modification of products for IVD diagnostics - Group C and D medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 30, 2024.
This page provides complete registration details including product code (1074-777), brand name (Siemens/Siemens Healtheneers), 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.
1) Atellica IM Toxoplasma lgG (Toxo G) 2) Atellica IM Toxoplasma lgG Quality Control (Toxo G QC) 3) Atellica IM Toxoplasma lgM (Toxo M) 4) Atellica IM Toxoplasma lgM Quality Control (Toxo M QC) 5) Atellica IM Cytomegalovirus lgG (CMVG) 6) Atellica IM CMV lgG Quality Control (CMV lgG QC) 7) Atellica IM CMV lgM (CMV lgM) assay 8) Atellica IM CMV lgM Quality Control (CMV lgM QC)