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Intravenous Flow Regulator - Argentina Medical Device Registration

Access comprehensive regulatory information for Intravenous Flow Regulator 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 09, 2024.

This page provides complete registration details including product code (261-5), brand name (Leventon), 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
Intravenous Flow Regulator
Regulador de Caudal Intravenoso
Argentina Medical Device Registration
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Product Information

Dose-Flow

Spanish:

Dosi-Flow

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
261-5
Brand Name
Leventon
Product Name
Intravenous Flow Regulator
Regulador de Caudal Intravenoso
Registration Information
Registration Date
April 09, 2024
Database ID
cmhaytn4r03z4ekuza1yk2gfz
Authorized Representative