2315-92Sirolimus Elution Resorbable Magnesium Coronary Scaffolding System
Argentina Medical Device Registration · BIOTRONIK · BIOTRONIK ARGENTINA SRL · Registered July 01, 2024
Registration Class III-IV- Registration Type
- Registration Class III-IV
- Registro Clase III-IV
- Product Code
- 2315-92
- Brand Name
- BIOTRONIK
- Product Name
- Sirolimus Elution Resorbable Magnesium Coronary Scaffolding System
- Sistema de armazón coronario de magnesio reabsorbible de elución de sirolimus
- Registration Date
- July 01, 2024
- Database ID
- cmhaytq4d07jrekuzb1worukq
443103 Freesolve 2.5/13 2.5 13 119 443108 Freesolve 3.0/13 3.0 13 132 443113 Freesolve 3.5/13 3.5 13 127 443118 Freesolve 4.0/13 4.0 13 136 443104 Freesolve 2.5/18 2.5 18 166 443109 Freesolve 3.0/18 3.0 18 172 443114 Freesolve 3.5/18 3.5 18 171 443119 Freesolve 4.0/18 4.0 18 188 443105 Freesolve 2.5/22 2.5 22 201 443110 Freesolve 3.0/22 3.0 22 212 443115 Freesolve 3.5/22 3.5 22 214 443120 Freesolve 4.0/22 4.0 22 240 482156 Freesolve 3.0/26 3.0 26 252 482157 Freesolve 3.5/26 3.5 26 257 482158 Freesolve 4.0/26 4.0 26 275 443111 Freesolve 3.0/30 3.0 30 292 443116 Freesolve 3.5/30 3.5 30 300 443121 Freesolve 4.0/30 4.0 30 327
Access comprehensive regulatory information for Sirolimus Elution Resorbable Magnesium Coronary Scaffolding System in the Argentina medical device market through Pure Global AI's free database. This Registration 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 01, 2024.
This page provides complete registration details including product code (2315-92), brand name (BIOTRONIK), 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.