921-50Resistance loss device
Argentina Medical Device Registration · PORTEX · AMERICAN FIURE S.A. · Registered January 16, 2024
Revalidation of Registration I-II-III-IV- Registration Type
- Revalidation of Registration I-II-III-IV
- Reválida de Registro I-II-III-IV
- Product Code
- 921-50
- Brand Name
- PORTEX
- Product Name
- Resistance loss device
- dispositivo de perdida de resistencia
- Registration Date
- January 16, 2024
- Database ID
- cmhaytt5j09e5ekuzlxraa3x7
100/398/000 Portex® Resistance loss device RESISTANCE LOSS DEVICE
100/398/000 Portex® Dispositivo de pérdida de resistencia DISPOSITIVO DE PÉRDIDA DE RESISTENCIA
Access comprehensive regulatory information for Resistance loss device in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on January 16, 2024.
This page provides complete registration details including product code (921-50), brand name (PORTEX), 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.