Ptosis Suspension Kit - Argentina Medical Device Registration

Access comprehensive regulatory information for Ptosis Suspension Kit in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on October 12, 2023.

This page provides complete registration details including product code (350-123), brand name (FCI), 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.