LIQUIFORM ALKALINE PHOSPHATASE - Argentina Medical Device Registration

Access comprehensive regulatory information for LIQUIFORM ALKALINE PHOSPHATASE 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 25, 2023.

This page provides complete registration details including product code (95-294), brand name (LIQUIFORM ALKALINE PHOSPHATASE), 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.