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Alinity c Ammonia Ultra Reagent Kit - Albania Medical Device Registration

Access comprehensive regulatory information for Alinity c Ammonia Ultra Reagent Kit in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Sentinel CH. S.p.A. Via Robert Koch, 2, Milano 20152, Italy. The device was registered on March 30, 2020.

This page provides complete registration details including product model (Alinity c Ammonia Ultra Reagent Kit 08P2220 (200tests)), 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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Alinity c Ammonia Ultra Reagent Kit
Albania Medical Device Registration
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Product Information

Eshte nje reagent qe perdoret per percaktimin sasior enzimatik te amoniakut ne serumin dhe plazmen humane nepermjet analizatoreve alinity

Device Classification
Risk Class
Invitro
Product Model
Alinity c Ammonia Ultra Reagent Kit 08P2220 (200tests)
Product Name
Alinity c Ammonia Ultra Reagent Kit
Registration Information
Registration Date
March 30, 2020
Analysis ID
6980