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Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713 - Albania Medical Device Registration

Access comprehensive regulatory information for Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713 in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Abbott Ireland Diagnostics Division Finisklin Business Park, Sligo, Ireland. The device was registered on July 06, 2022.

This page provides complete registration details including product model (Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713), 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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Invitro
Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713
Albania Medical Device Registration
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Product Information

Reagent, kalibrator dhe kontrolle per percaktimin sasior te antitrupave IgM te prodhuaar kunder virusit te Rubelles

Device Classification
Risk Class
Invitro
Product Model
Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713
Product Name
Alinity Rubella IgM Reagent Kit: 08P4722; 08P4732; Alinity Rubella IgM Calibrator - 08P4701; Alinity Rubella IgM Controls: 08P4710; 08P4713
Registration Information
Registration Date
July 06, 2022
Analysis ID
12285