8162Alinity c Uric Reagent Kit 08P5620; Alinity c Uric Reagent Kit 08P5630;
Albania medical device registration · Abbott GmbH& Co.KG Max-Planck-Ring 2, 65205 Wiesbaden Germany · Invitro · Model Alinity c Uric Reagent Kit 08P5620 (1200 tests); Alinity c Uric Reagent Kit 08P5630 (5000 tests); · Registered October 05, 2020
- Risk Class
- Invitro
- Product Model
- Alinity c Uric Reagent Kit 08P5620 (1200 tests); Alinity c Uric Reagent Kit 08P5630 (5000 tests);
- Product Name
- Alinity c Uric Reagent Kit 08P5620; Alinity c Uric Reagent Kit 08P5630;
- Registration Date
- October 05, 2020
- Analysis ID
- 8162
Analize qe perdoren per percaktimin sasion te acidit urik ne serumin njerezor, ne urine dhe ne plazem.
Access comprehensive regulatory information for Alinity c Uric Reagent Kit 08P5620; Alinity c Uric Reagent Kit 08P5630; 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 c Uric Reagent Kit 08P5620 (1200 tests); Alinity c Uric Reagent Kit 08P5630 (5000 tests); ), 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.