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Gama GT Liquiform - Argentina Medical Device Registration

Access comprehensive regulatory information for Gama GT Liquiform in the Argentina medical device market through Pure Global AI's free database. This IVD Registration Group A and B 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 (95-311), brand name (Gama GT Liquiform), 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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IVD Registration Group A and B
Gama GT Liquiform
Argentina Medical Device Registration
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Product Information

Gama GT Liquiform (Gama-Glutamil Transpeptidasa (GGT))

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
95-311
Brand Name
Gama GT Liquiform
Product Name
Gama GT Liquiform
Registration Information
Registration Date
June 25, 2024
Database ID
cmhayu5bh0kpzekuz4a0rl10q
Authorized Representative