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Alinity i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732 - Albania Medical Device Registration

Access comprehensive regulatory information for Alinity i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732 in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Abbott Ireland Diagnostic Division, Lisnamuck, Longford, Co.Longford , Ireland. The device was registered on March 24, 2020.

This page provides complete registration details including product model (Alinity i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732), 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 i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732
Albania Medical Device Registration
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Device Classification
Risk Class
Invitro
Product Model
Alinity i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732
Product Name
Alinity i B12 Calibrators 07P6701; Alinity i B12 Controls 07P6710; Alinity i B12 Reagent Kit 07P6722; Alinity i B12 Reagent Kit 07P6732
Registration Information
Registration Date
March 24, 2020
Analysis ID
6881