QIAstat-Dx® Respiratory SARS-CoV-2 Panel
Argentina Medical Device Registration · QIAGEN · TECNOLAB S.A. · Registered July 05, 2024
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
- 1252-214
- Brand Name
- QIAGEN
- Product Name
- QIAstat-Dx® Respiratory SARS-CoV-2 Panel
- Registration Date
- July 05, 2024
- Database ID
- cmhayu5bd0kbdekuz8ljpmexf
- Name
- TECNOLAB S.A.
Catalogue number: 691214
N° de catálogo: 691214
Access comprehensive regulatory information for QIAstat-Dx® Respiratory SARS-CoV-2 Panel 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 July 05, 2024.
This page provides complete registration details including product code (1252-214), brand name (QIAGEN), 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.