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Alinity i CA 15-3 Reagent Kit 08P5130 ; Alinity i CA 15-3 Reagent Kit 08P5020 ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110; - Albania Medical Device Registration

Access comprehensive regulatory information for Alinity i CA 15-3 Reagent Kit 08P5130 ; Alinity i CA 15-3 Reagent Kit 08P5020 ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110; 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 CA 15-3 Reagent Kit 08P5130 (1000 tests); Alinity i CA 15-3 Reagent Kit 08P5120 (200 tests) ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110; ), 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.

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Albania Official Data
Invitro
Alinity i CA 15-3 Reagent Kit 08P5130 ; Alinity i CA 15-3 Reagent Kit 08P5020 ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110;
Albania Medical Device Registration
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Device Classification
Risk Class
Invitro
Product Model
Alinity i CA 15-3 Reagent Kit 08P5130 (1000 tests); Alinity i CA 15-3 Reagent Kit 08P5120 (200 tests) ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110;
Product Name
Alinity i CA 15-3 Reagent Kit 08P5130 ; Alinity i CA 15-3 Reagent Kit 08P5020 ; Alinity i CA 15-3 Calibrators 08P5101; Alinity i CA 15-3 Controls 08P5110;
Registration Information
Registration Date
October 05, 2020
Analysis ID
8164