921-47Epidural Filter
Argentina Medical Device Registration · PORTEX · AMERICAN FIURE S.A. · Registered April 15, 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
- 921-47
- Brand Name
- PORTEX
- Product Name
- Epidural Filter
- Filtro Epidural
- Registration Date
- April 15, 2024
- Database ID
- cmhayu0e40eziekuz0vsyq7kb
100/386/010CZ flat Portex epidural filter with rotator neck - adapted Luer closure
100/386/010CZ filtro chato epidural Portex con cuello rotador - cierre Luer adaptado
Access comprehensive regulatory information for Epidural Filter 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 April 15, 2024.
This page provides complete registration details including product code (921-47), 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.