Albania AKBPM registration 6618SilverGraft
AlbaniaAesculap AG Am Aesculap-Platz 78532 Tuttlingen GermanyIIIModel Silver Graft (sipas listes se bashkengjitur)Registered January 20, 2020
VerifiedAKBPM · official registry
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
Product information
Grafte vaskulare te implantueshme, perdorim ne kirurgjine vaskulare
About this record
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.