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HDL LE - Argentina Medical Device Registration

Access comprehensive regulatory information for HDL LE 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 26, 2024.

This page provides complete registration details including product code (95-310), brand name (HDL LE), 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
HDL LE
Argentina Medical Device Registration
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Product Information

HDL LE. (High-Density Lipoprotein (HDL))

Spanish:

HDL LE. (Lipoproteína de Alta Densidad (HDL))

Device Classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
95-310
Brand Name
HDL LE
Product Name
HDL LE
Registration Information
Registration Date
June 26, 2024
Database ID
cmhaytq4e07kmekuzq0tvjcv3
Documents
Authorized Representative