Alinity i Toxo IgG Reagent Kit (2x100 Tests) 07P4522; Alinity i Toxo IgG Reagent Kit (2x500 Tests) 07P4532 ; Alinity i Toxo IgG Calibrators 07P4501; Alinity i Toxo IgG Controls 07P4510 - Albania Medical Device Registration
Access comprehensive regulatory information for Alinity i Toxo IgG Reagent Kit (2x100 Tests) 07P4522; Alinity i Toxo IgG Reagent Kit (2x500 Tests) 07P4532 ; Alinity i Toxo IgG Calibrators 07P4501; Alinity i Toxo IgG Controls 07P4510 in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Abbott GmbH & Co.KG Max-Planck-Ring 2 65205 Wiesbaden Germany. The device was registered on February 20, 2020.
This page provides complete registration details including product model (Alinity i Toxo IgG Reagent Kit (2x100 Tests) 07P4522; Alinity i Toxo IgG Reagent Kit (2x500 Tests) 07P4532 ; Alinity i Toxo IgG Calibrators 07P4501; Alinity i Toxo IgG Controls 07P4510 ), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.
Analiza e Toxo IgG eshte nje imunoanalize mikrogrimcash kemilumineshente (CMIA) e perdorur per percaktimin sasior te antitrupave IgG te Toxoplasma gondii ne serumin human dhe plazem ne analizuesin Alinity. Kontrollet e Toxo IgG perdoren per kontrollin e precizionit te saktesise se testit per analizen sasiore te antitrupave IgG te Toxoplasma gondii ne serumin human dhe plazem ne analizuesin Alinity.