THE PACK AIA 900 - Argentina Medical Device Registration
Access comprehensive regulatory information for THE PACK AIA 900 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 July 03, 2024.
This page provides complete registration details including product code (908-249), brand name (THE PACK AIA 900), 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.
a) AIA-900 b) AIA-900 9 Tray sorter c) AIA-900 19 Tray sorter d) ST AIA-PACK hsE2 e) ST AIA-PACK hsE2 CALIBRATOR SET f) ST AIA-PACK hsE2 SAMPLE DILUTING SOLUTION g) ST AIA-PACK PROGIII h) ST AIA-PACK PROGIII CALIBRATOR SET i) ST AIA-PACK PROGIII SAMPLE DILUTING SOLUTION j) ST AIA-PACK C-Peptide II k) ST AIA-PACK C-Peptide II CALIBRATOR SET l) ST AIA-PACK C-Peptide II SAMPLE DILUTING SOLUTION m) AIA-PACK C-Peptide CONTROL SET n ST AIA-PACK Homocysteine o) ST AIA-PACK Homocysteine CALIBRATOR SET p) ST AIA-PACK Homocysteine SAMPLE DILUTING SOLUTION q) ST AIA-PACK Homocysteine PRETREATMENT SET r) AIA-PACK Homocysteine CONTROL SET