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Allplex™ CT/NG/MG/TV Assay - Argentina Medical Device Registration

Access comprehensive regulatory information for Allplex™ CT/NG/MG/TV Assay in the Argentina medical device market through Pure Global AI's free database. This Non-agile modification 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 December 20, 2023.

This page provides complete registration details including product code (626-170), brand name (Seegene), 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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Non-agile modification of products for IVD diagnostics - Group C and D
Allplex™ CT/NG/MG/TV Assay
Argentina Medical Device Registration
Pure Global
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Product Information

Allplex™ CT/NG/MG/TV Assay (Ref.: SD9400X for 100 reactions). Allplex™ CT/NG/MG/TV Assay (Ref.: SD9400Y for 50 reactions).

Spanish:

Allplex™ CT/NG/MG/TV Assay (Ref.: SD9400X para 100 reacciones). Allplex™ CT/NG/MG/TV Assay (Ref.: SD9400Y para 50 reacciones).

Device Classification
Registration Type
Non-agile modification of products for IVD diagnostics - Group C and D
Modificación NO Ágil De Productos Para Diagnóstico IVD - Grupo C Y D
Product Code
626-170
Brand Name
Seegene
Product Name
Allplex™ CT/NG/MG/TV Assay
Registration Information
Registration Date
December 20, 2023
Database ID
cmhayubdn0p6hekuzpw6byf4o
Authorized Representative