Argentina flag661-100

Set de Plasmafiltro

Argentina Medical Device Registration · Prismaflex · DROGUERIA COMARSA S.A. · Registered June 08, 2024

Revalidation of Registration I-II-III-IV
Device classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
661-100
Brand Name
Prismaflex
Product Name
Set de Plasmafiltro
Registration information
Registration Date
June 08, 2024
Database ID
cmhaytq4f07olekuzpps1fjpu
Authorized representative
Documents
Product information

Set Prismaflex TPE 1000; Set Prismaflex TPE 2000

About this record

Access comprehensive regulatory information for Set de Plasmafiltro 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 June 08, 2024.

This page provides complete registration details including product code (661-100), brand name (Prismaflex), 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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