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LIQUID EMBOLIC AGENT - Argentina Medical Device Registration

Access comprehensive regulatory information for LIQUID EMBOLIC AGENT 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 25, 2024.

This page provides complete registration details including product code (799-69), brand name (SQUID), 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
LIQUID EMBOLIC AGENT
AGENTE EMBÓLICO LÍQUIDO
Argentina Medical Device Registration
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Product Information

SQUID12, SQUID12LD, SQUID18, SQUID18LD, SQUID34, SQUID34LD, SQUID12_3, SQUID12LD_3, SQUID18_3, SQUID18LD_3, SQUID34_3, SQUID34LD_3, SQUIDPERI12, SQUIDPERI12LD, SQUIDPERI18, SQUIDPERI18LD, SQUIDPERI34, SQUIDPERI34LD, SQUIDPERI12_3, SQUIDPERI12LD_3, SQUIDPERI18_3, SQUIDPERI18LD_3, SQUIDPERI34_3, SQUIDPERI34LD_3

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
799-69
Brand Name
SQUID
Product Name
LIQUID EMBOLIC AGENT
AGENTE EMBÓLICO LÍQUIDO
Registration Information
Registration Date
June 25, 2024
Database ID
cmhayu5bh0kqdekuzsxy2tf6l
Documents
Authorized Representative