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Alinity i CA 125 II Reagent Kit 08P4920 ; Alinity i CA 125 II Reagent Kit 08P4930 ; Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910; - Albania Medical Device Registration

Access comprehensive regulatory information for Alinity i CA 125 II Reagent Kit 08P4920 ; Alinity i CA 125 II Reagent Kit 08P4930 ; Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910; 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 125 II Reagent Kit 08P4920 (200 tests); Alinity i CA 125 II Reagent Kit 08P4930 (1000 tests); Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910; ), 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 125 II Reagent Kit 08P4920 ; Alinity i CA 125 II Reagent Kit 08P4930 ; Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910;
Albania Medical Device Registration
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Product Information

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Device Classification
Risk Class
Invitro
Product Model
Alinity i CA 125 II Reagent Kit 08P4920 (200 tests); Alinity i CA 125 II Reagent Kit 08P4930 (1000 tests); Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910;
Product Name
Alinity i CA 125 II Reagent Kit 08P4920 ; Alinity i CA 125 II Reagent Kit 08P4930 ; Alinity i CA 125 II Calibrators 08P4901; Alinity i CA 125 II Controls 08P4910;
Registration Information
Registration Date
October 05, 2020
Analysis ID
8165