1252-215artus® SARS-CoV-2 Prep&Amp UM Kit
Argentina Medical Device Registration · artus® SARS-CoV-2 Prep&Amp UM Kit · TECNOLAB S.A. · Registered April 11, 2024
IVD Modification Group A and B- Registration Type
- IVD Modification Group A and B
- Modificación IVD Grupo A y B
- Product Code
- 1252-215
- Brand Name
- artus® SARS-CoV-2 Prep&Amp UM Kit
- Product Name
- artus® SARS-CoV-2 Prep&Amp UM Kit
- Registration Date
- April 11, 2024
- Database ID
- cmhayu0e40f0nekuzu5cnng7w
- Name
- TECNOLAB S.A.
Catalogue number: 4511460 (for 768 determinations). Catalogue number: 4511469 (for 3072 determinations).
N° Catálogo: 4511460 (por 768 determinaciones). N° Catálogo: 4511469 (por 3072 determinaciones).
Access comprehensive regulatory information for artus® SARS-CoV-2 Prep&Amp UM Kit in the Argentina medical device market through Pure Global AI's free database. This IVD Modification 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 April 11, 2024.
This page provides complete registration details including product code (1252-215), brand name (artus® SARS-CoV-2 Prep&Amp UM Kit), 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.