SilverGraft - Albania Medical Device Registration
Access comprehensive regulatory information for SilverGraft in the Albania medical device market through Pure Global AI's free database. This III medical device is manufactured by Aesculap AG Am Aesculap-Platz 78532 Tuttlingen Germany. The device was registered on January 20, 2020.
This page provides complete registration details including product model (Silver Graft (sipas listes se bashkengjitur)), 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
III
SilverGraft
Albania Medical Device Registration
Product Information
Grafte vaskulare te implantueshme, perdorim ne kirurgjine vaskulare
Device Classification
Risk Class
III
Product Model
Silver Graft (sipas listes se bashkengjitur)
Product Name
SilverGraft
Registration Information
Registration Date
January 20, 2020
Analysis ID
6618
Manufacturer