ENDOVASCULAR COAGULATION SYSTEM - Argentina Medical Device Registration
Access comprehensive regulatory information for ENDOVASCULAR COAGULATION SYSTEM 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 July 26, 2024.
This page provides complete registration details including product code (1991-238), brand name (VENCLOSE), 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.
MANUFACTURER 1 & 2: DigiRF VencloseTM Generator: VC-RFG-1 VencloseTM Power Cord: VC-PC-B, VC-PC-E, VC-PC-G, VC-PC-C, VC-PC-I, VC-PC-N, VC-PC-L, VC-PC-K, VC-PC-M, VC-PC-H, VC-PC-J, VC-PC-A. MANUFACTURER 1 & 3: VencloseTM Pedal: VC-FP-1 MANUFACTURER 1 & 4: VencloseTM RF ABLATION Catheter: VC-10A2.5.6F-100 and VC-10A2.5-6F-60 Venclose MavenTM Catheter: VC-0.5-6F
FABRICANTE 1 y 2: Generador DigiRF VencloseTM: VC-RFG-1 Cable de Alimentación VencloseTM: VC-PC-B, VC-PC-E, VC-PC-G, VC-PC-C, VC-PC-I, VC-PC-N, VC-PC-L, VC-PC-K, VC-PC-M, VC-PC-H, VC-PC-J, VC-PC-A. FABRICANTE 1 y 3: Pedal VencloseTM: VC-FP-1 FABRICANTE 1 y 4: Catéter de ablación VencloseTM RF: VC-10A2.5.6F-100 y VC-10A2.5-6F-60 Catéter Venclose MavenTM: VC-0.5-6F