669-269Ventricular Drainage Catheter
Argentina Medical Device Registration · Spiegelberg · B BRAUN MEDICAL S.A. · Registered July 10, 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
- 669-269
- Brand Name
- Spiegelberg
- Product Name
- Ventricular Drainage Catheter
- Catéter de Drenaje Ventricular
- Registration Date
- July 10, 2024
- Database ID
- cmhayu5bd0ka6ekuz7ks5b9kg
Ventricular Drainage Catheter 8F EVD30.010.01 Ventricular Drainage Catheter with Cranial Ligation 8F EVD30.014.01 Ventricular Drainage Catheter 10F EVD30.030.01 Ventricular Drainage Catheter with Cranial Ligation 10F EVD30.034.01 Silverline® EVD30.010.02 8F Ventricular Drainage Catheter Ventricular Drainage Catheter with Cranial Ligation 8F Silverline® EVD30.014.02 Silverline® EVD30.015.02 8F Subdural Drainage Catheter Ventricular Drainage Catheter 6F Silverline® EVD30.020.02 Ventricular Drainage Catheter 10F Silverline® EVD30.030.02 Ventricular Drainage Catheter with Cranial Ligation 10F Silverline® EVD30.034.02 Silverline® EVD30.035.02 10F Subdural Drainage Catheter
Catéter de Drenaje Ventricular 8F EVD30.010.01 Catéter de Drenaje Ventricular con ligadura craniana 8F EVD30.014.01 Catéter de Drenaje Ventricular 10F EVD30.030.01 Catéter de Drenaje Ventricular con ligadura craniana 10F EVD30.034.01 Catéter de Drenaje Ventricular 8F Silverline® EVD30.010.02 Catéter de Drenaje Ventricular con ligadura craniana 8F Silverline® EVD30.014.02 Catéter de Drenaje Subdural 8F Silverline® EVD30.015.02 Catéter de Drenaje Ventricular 6F Silverline® EVD30.020.02 Catéter de Drenaje Ventricular 10F Silverline® EVD30.030.02 Catéter de Drenaje Ventricular con ligadura craniana 10F Silverline® EVD30.034.02 Catéter de Drenaje Subdural 10F Silverline® EVD30.035.02
Access comprehensive regulatory information for Ventricular Drainage Catheter 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 July 10, 2024.
This page provides complete registration details including product code (669-269), brand name (Spiegelberg), 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.