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Allplex STI Essential Assay - Argentina Medical Device Registration

Access comprehensive regulatory information for Allplex STI Essential 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 September 20, 2023.

This page provides complete registration details including product code (626-166), 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 STI Essential Assay
Argentina Medical Device Registration
Pure Global
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Pricing
Product Information

- Allplex STI Essential Assay (SD10245Z) x 25 determinations. - Allplex STI Essential Assay (SD9801Y) x 50 determinations. - Allplex STI Essential Assay (SD9801X) x 100 determinations.

Spanish:

- Allplex STI Essential Assay (SD10245Z) x 25 determinaciones. - Allplex STI Essential Assay (SD9801Y) x 50 determinaciones. - Allplex STI Essential Assay (SD9801X) x 100 determinaciones.

Device Classification
Registration Type
Non-agile modification of products for IVD diagnostics - Group C and D
Modificaciรณn NO รgil De Productos Para Diagnรณstico IVD - Grupo C Y D
Product Code
626-166
Brand Name
Seegene
Product Name
Allplex STI Essential Assay
Registration Information
Registration Date
September 20, 2023
Database ID
cmhaytt5q09z9ekuza0zwnpp8
Authorized Representative