Argentina flag1252-226

AESKUBLOTS® product family and HELIA® instrument

Familia de productos AESKUBLOTS® e instrumento HELIA®

Argentina Medical Device Registration · AESKUBLOTS® product family and HELIA® instrument · TECNOLAB S.A. · Registered June 18, 2024

IVD Registration Group A and B
Device classification
Registration Type
IVD Registration Group A and B
Registro IVD Grupo A y B
Product Code
1252-226
Brand Name
AESKUBLOTS® product family and HELIA® instrument
Familia de productos AESKUBLOTS® e instrumento HELIA®
Product Name
AESKUBLOTS® product family and HELIA® instrument
Familia de productos AESKUBLOTS® e instrumento HELIA®
Registration information
Registration Date
June 18, 2024
Database ID
cmhayu5bh0kr3ekuzjtt0cozq
Authorized representative
Documents
Product information

AESKUBLOTS® reagents 1) AESKUBLOTS® ANA-17 Pro (Reference: 4001) 2) AESKUBLOTS® Vasculitis Pro (Reference: 4002) 3) AESKUBLOTS® Liver Pro (Reference: 4004) 4) AESKUBLOTS® Gastro Pro (Reference: 4005) 5) AESKUBLOTS® ANA-17 Comp (Reference: 4008) Analyzers 6) HELIA® Automated BLOT System (Reference: REF. LIA-1000)

Spanish:

Reactivos AESKUBLOTS® 1) AESKUBLOTS® ANA-17 Pro (Referencia: 4001) 2) AESKUBLOTS® Vasculitis Pro (Referencia: 4002) 3) AESKUBLOTS® Liver Pro (Referencia: 4004) 4) AESKUBLOTS® Gastro Pro (Referencia: 4005) 5) AESKUBLOTS® ANA-17 Comp (Referencia: 4008) Analizadores 6) HELIA® Automated BLOT System (Referencia: REF.LIA-1000)

About this record

Access comprehensive regulatory information for AESKUBLOTS® product family and HELIA® instrument 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 18, 2024.

This page provides complete registration details including product code (1252-226), brand name (AESKUBLOTS® product family and HELIA® instrument), 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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