Allplex™ GI-Helminth(I) Assay
Argentina Medical Device Registration · Allplex™ GI-Helminth(I) Assay · BIOSYSTEMS S.A. · Registered August 16, 2023
IVD Registration Group A and B- Registration Type
- IVD Registration Group A and B
- Registro IVD Grupo A y B
- Product Code
- 626-203
- Brand Name
- Allplex™ GI-Helminth(I) Assay
- Product Name
- Allplex™ GI-Helminth(I) Assay
- Registration Date
- August 16, 2023
- Database ID
- cmhayu2zg0hweekuzj5go37lq
- Name
- BIOSYSTEMS S.A.
- Allplex™ GI-Helminth(I) Assay (GI10189Z) x 25 determinations. - Allplex™ GI-Helminth(I) Assay (GI10190Y) x 50 determinations. - Allplex™ GI-Helminth(I) Assay (GI10191X) x 100 determinations.
- Allplex™ GI-Helminth(I) Assay (GI10189Z) x 25 determinaciones. - Allplex™ GI-Helminth(I) Assay (GI10190Y) x 50 determinaciones. - Allplex™ GI-Helminth(I) Assay (GI10191X) x 100 determinaciones.
Access comprehensive regulatory information for Allplex™ GI-Helminth(I) Assay in the Argentina medical device market through Pure Global AI's free database. This IVD Registration Group A and B 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 (626-203), brand name (Allplex™ GI-Helminth(I) Assay), 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.