1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent
Argentina Medical Device Registration · 1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent · WM ARGENTINA S.A. · Registered June 06, 2024
IVD Modification Group A and B- Registration Type
- IVD Modification Group A and B
- Modificación IVD Grupo A y B
- Product Code
- 794-481
- Brand Name
- 1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent
- Product Name
- 1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent
- Registration Date
- June 06, 2024
- Database ID
- cmhaytsdm08n2ekuza94ihkjj
Not applicable
No aplica
Access comprehensive regulatory information for 1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent 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 June 06, 2024.
This page provides complete registration details including product code (794-481), brand name (1)LIAISON ® N-TACT® PTH Gen II 2)LIAISON ® N-TACT® PTH Gen II Control Set 3)LIAISON ® N-TACT® PTH Gen II Specimen Diluent), 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.