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HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma) - Argentina Medical Device Registration

Access comprehensive regulatory information for HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma) in the Argentina medical device market through Pure Global AI's free database. This Registration of products for IVD diagnostics - Group C and D medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on May 13, 2024.

This page provides complete registration details including product code (1275-287), brand name (Abbott), 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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Registration of products for IVD diagnostics - Group C and D
HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma)
Argentina Medical Device Registration
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Device Classification
Registration Type
Registration of products for IVD diagnostics - Group C and D
Registro De Productos Para Diagnรณstico IVD - Grupo C Y D
Product Code
1275-287
Brand Name
Abbott
Product Name
HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma)
Registration Information
Registration Date
May 13, 2024
Database ID
cmhaytks301wsekuzzr2hkrmm
Documents
Authorized Representative