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Hemodiafiltros - Argentina Medical Device Registration

Access comprehensive regulatory information for Hemodiafiltros in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 23, 2024.

This page provides complete registration details including product code (169-93), brand name (Fresenius Medical Care), 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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Registration modification (non-agile) Class III-IV
Hemodiafiltros
Argentina Medical Device Registration
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Product Information

1) FX600HDF (See manufacturer 1, 2, 3 and 4) 2) FX800HDF (See manufacturer 1, 2, 3 and 4) 3) FX1000HDF (See manufacturer 1, 2 and 3)

Spanish:

1) FX600HDF (Ver fabricante 1, 2, 3 y 4) 2) FX800HDF (Ver fabricante 1, 2, 3 y 4) 3) FX1000HDF (Ver fabricante 1, 2 y 3)

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificación de Registro (no ágil) Clase III-IV
Product Code
169-93
Brand Name
Fresenius Medical Care
Product Name
Hemodiafiltros
Registration Information
Registration Date
June 23, 2024
Database ID
cmhaytq4e07lnekuzscmj3toe
Documents
Authorized Representative