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CA 125 II - Albania Medical Device Registration

Access comprehensive regulatory information for CA 125 II in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Roche Diagnostics GmbH, Roche Proffesional Diagnostics Sandhofer Strasse 116 D-68305 Mannheim. The device was registered on February 03, 2018.

This page provides complete registration details including product model (CA 125 II 11776223), 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
CA 125 II
Albania Medical Device Registration
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Product Information

Reagent imunologjik per diagnostikim in vitro per percaktimin sasior te percaktuesve reaktive OC 125 ne serum dhe plazme njerezore

Device Classification
Risk Class
Invitro
Product Model
CA 125 II 11776223
Product Name
CA 125 II
Registration Information
Registration Date
February 03, 2018
Analysis ID
3278