Allplex STI Essential Assay
Argentina Medical Device Registration · Seegene · BIOSYSTEMS S.A. · Registered September 20, 2023
Non-agile modification of products for IVD diagnostics - Group C and D- 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
- 626-166
- Brand Name
- Seegene
- Product Name
- Allplex STI Essential Assay
- Registration Date
- September 20, 2023
- Database ID
- cmhaytt5q09z9ekuza0zwnpp8
- Name
- BIOSYSTEMS S.A.
- Allplex STI Essential Assay (SD10245Z) x 25 determinations. - Allplex STI Essential Assay (SD9801Y) x 50 determinations. - Allplex STI Essential Assay (SD9801X) x 100 determinations.
- Allplex STI Essential Assay (SD10245Z) x 25 determinaciones. - Allplex STI Essential Assay (SD9801Y) x 50 determinaciones. - Allplex STI Essential Assay (SD9801X) x 100 determinaciones.
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.