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Pump Syringe - Argentina Medical Device Registration

Access comprehensive regulatory information for Pump Syringe 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 July 30, 2024.

This page provides complete registration details including product code (634-260), brand name (PENTAFERTE), 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
Bilingual (Spanish/English)
Revalidation of Registration I-II-III-IV
Pump Syringe
Jeringa de bomba
Argentina Medical Device Registration
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Product Information

10ml L/L syringe without needle 002022620F 20ml L/L syringe without needle 002022720F 60ml L/L syringe without needle 002022970F

Spanish:

Jeringa L/L de 10ml sin aguja 002022620F Jeringa L/L de 20ml sin aguja 002022720F Jeringa L/L de 60ml sin aguja 002022970F

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
634-260
Brand Name
PENTAFERTE
Product Name
Pump Syringe
Jeringa de bomba
Registration Information
Registration Date
July 30, 2024
Database ID
cmhayu5bf0khzekuz7iefl976
Authorized Representative