Albania AKBPM registration 6998Silver Graft
AlbaniaAesculap AG Am Aesculap-Platz 78532 Tuttlingen GermanyIIIModel SIlverGraft (Sipas listës bashkangjitur)Registered March 30, 2020
VerifiedAKBPM · official registry
Device classification
- Risk Class
- III
- Product Model
- SIlverGraft (Sipas listës bashkangjitur)
- Product Name
- Silver Graft
Registration information
- Registration Date
- March 30, 2020
- Analysis ID
- 6998
Manufacturer
Product information
Grafte vaskulare per kirurgjine vaskulare
About this record
Access comprehensive regulatory information for Silver Graft 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 March 30, 2020.
This page provides complete registration details including product model (SIlverGraft (Sipas listës bashkangjitur)), 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.