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Anesthesia equipment - Argentina Medical Device Registration

Access comprehensive regulatory information for Anesthesia equipment 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 23, 2024.

This page provides complete registration details including product code (1601-43), brand name (Drรคger), 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
Anesthesia equipment
Equipo para administrar anestesia
Argentina Medical Device Registration
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Product Information

1) Fabius Plus, 2) fabius Plus XL.

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
1601-43
Brand Name
Drรคger
Product Name
Anesthesia equipment
Equipo para administrar anestesia
Registration Information
Registration Date
June 23, 2024
Database ID
cmhayu5bh0kr0ekuz7otagwf5
Authorized Representative