626-213Allplex™ Entero-DR Assay
Argentina Medical Device Registration · Seegene · BIOSYSTEMS S.A. · Registered April 29, 2024
Registration of products for IVD diagnostics - Group C and D- Registration Type
- Registration of products for IVD diagnostics - Group C and D
- Registro De Productos Para Diagnóstico IVD - Grupo C Y D
- Product Code
- 626-213
- Brand Name
- Seegene
- Product Name
- Allplex™ Entero-DR Assay
- Registration Date
- April 29, 2024
- Database ID
- cmhayu0e30ex3ekuz5i8zj7nf
- Name
- BIOSYSTEMS S.A.
1) Allplex™ Entero-DR Assay (CR10384Z) x 25 determinaciones. 2) Allplex™ Entero-DR Assay (CR9700X) x 100 determinaciones.
Access comprehensive regulatory information for Allplex™ Entero-DR 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 April 29, 2024.
This page provides complete registration details including product code (626-213), 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.