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Chikungunya IgG/IgM Rapid Test - Argentina Medical Device Registration

Access comprehensive regulatory information for Chikungunya IgG/IgM Rapid Test 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 April 26, 2024.

This page provides complete registration details including product code (2123-117), brand name (Chikungunya IgG/IgM Rapid Test), 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
Chikungunya IgG/IgM Rapid Test
Argentina Medical Device Registration
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Product Information

Chikungunya IgG/IgM Rapid Test

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
2123-117
Brand Name
Chikungunya IgG/IgM Rapid Test
Product Name
Chikungunya IgG/IgM Rapid Test
Registration Information
Registration Date
April 26, 2024
Database ID
cmhayu0e30exnekuzdjy9u7s3
Authorized Representative