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Syphilis Ultra Rapid Test Device (Whole Blood/Serum/ Plasma) - Argentina Medical Device Registration

Access comprehensive regulatory information for Syphilis Ultra 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 August 10, 2023.

This page provides complete registration details including product code (1275-285), 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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Registration of products for IVD diagnostics - Group C and D
Syphilis Ultra 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
1275-285
Brand Name
Abbott
Product Name
Syphilis Ultra Rapid Test Device (Whole Blood/Serum/ Plasma)
Registration Information
Registration Date
August 10, 2023
Database ID
cmhaytnv904vkekuz8alal4pj
Documents
Authorized Representative