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Synthetic hollow fiber dialysis filter - Argentina Medical Device Registration

Access comprehensive regulatory information for Synthetic hollow fiber dialysis 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 February 23, 2024.

This page provides complete registration details including product code (877-40), brand name (Nipro), 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
Synthetic hollow fiber dialysis filter
Filtro para diรกlisis de fibra hueca sintรฉtico
Argentina Medical Device Registration
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Product Information

ELISIO-110H, ELISIO-130H, ELISIO 150H, ELISIO-170H, ELISIO-190H, ELISIO-210H.

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
877-40
Brand Name
Nipro
Product Name
Synthetic hollow fiber dialysis filter
Filtro para diรกlisis de fibra hueca sintรฉtico
Registration Information
Registration Date
February 23, 2024
Database ID
cmhaytp5q06h9ekuzkyvmh07d
Authorized Representative