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Epidural Filter - Argentina Medical Device Registration

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.

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Argentina ANMAT Data
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Revalidation of Registration I-II-III-IV
Epidural Filter
Filtro Epidural
Argentina Medical Device Registration
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Product Information

100/386/010CZ flat Portex epidural filter with rotator neck - adapted Luer closure

Spanish:

100/386/010CZ filtro chato epidural Portex con cuello rotador - cierre Luer adaptado

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
921-47
Brand Name
PORTEX
Product Name
Epidural Filter
Filtro Epidural
Registration Information
Registration Date
April 15, 2024
Database ID
cmhayu0e40eziekuz0vsyq7kb
Authorized Representative