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Allplex ™ Vaginitis Screening Assay - Argentina Medical Device Registration

Access comprehensive regulatory information for Allplex ™ Vaginitis Screening Assay 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 16, 2023.

This page provides complete registration details including product code (626-167), 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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Registration of products for IVD diagnostics - Group C and D
Allplex ™ Vaginitis Screening Assay
Argentina Medical Device Registration
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Product Information

Allplex ™ Vaginitis Screening Assay (Ref.: SD9750Y) for 50 reactions. Allplex ™ Vaginitis Screening Assay (Ref.: SD9750X) for 100 reactions.

Spanish:

Allplex ™ Vaginitis Screening Assay (Ref.: SD9750Y) para 50 reacciones. Allplex ™ Vaginitis Screening Assay (Ref.: SD9750X) para 100 reacciones.

Device Classification
Registration Type
Registration of products for IVD diagnostics - Group C and D
Registro De Productos Para Diagnóstico IVD - Grupo C Y D
Product Code
626-167
Brand Name
Seegene
Product Name
Allplex ™ Vaginitis Screening Assay
Registration Information
Registration Date
August 16, 2023
Database ID
cmhayu2zf0hvqekuz4rf8oa2g
Documents
Authorized Representative