8163Alinity i HE4 Reagent Kit 08P5022 ; Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010
Albania medical device registration · Abbott GmbH& Co.KG Max-Planck-Ring 2, 65205 Wiesbaden Germany · Invitro · Model Alinity i HE4 Reagent Kit 08P5022 (200 tests); Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010 · Registered October 05, 2020
- Risk Class
- Invitro
- Product Model
- Alinity i HE4 Reagent Kit 08P5022 (200 tests); Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010
- Product Name
- Alinity i HE4 Reagent Kit 08P5022 ; Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010
- Registration Date
- October 05, 2020
- Analysis ID
- 8163
Imunoanalize mikrogrimcash kemilumineshente qe perdoren per percaktimin sasion te antigjenit HE4 ne serumin njerezor.
Access comprehensive regulatory information for Alinity i HE4 Reagent Kit 08P5022 ; Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010 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 October 05, 2020.
This page provides complete registration details including product model (Alinity i HE4 Reagent Kit 08P5022 (200 tests); Alinity i HE4 Calibrators 08P5001; Alinity i HE4 Controls 08P5010), 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.