Albania AKBPM registration 10022Implants, Instruments, Containers, Devices, Suture Material, Tissue Adhesives snd Procedure Kits (sipas listes bashkengjitur)
- Risk Class
- I;IIa;IIb
- Product Model
- Implants, Instruments, Containers, Devices, Suture Material, Tissue Adhesives snd Procedure Kits (sipas listes bashkengjitur)
- Product Name
- Implants, Instruments, Containers, Devices, Suture Material, Tissue Adhesives snd Procedure Kits (sipas listes bashkengjitur)
- Registration Date
- August 20, 2021
- Analysis ID
- 10022
Instrumenta dhe aksesore kirurgjikale, perdorim ne kirurgji te pergjithshme.
Access comprehensive regulatory information for Implants, Instruments, Containers, Devices, Suture Material, Tissue Adhesives snd Procedure Kits (sipas listes bashkengjitur) in the Albania medical device market through Pure Global AI's free database. This I;IIa;IIb medical device is manufactured by Aesculap AG Am Aesculap-Platz 78532 Tuttlingen Germany. The device was registered on August 20, 2021.
This page provides complete registration details including product model (Implants, Instruments, Containers, Devices, Suture Material, Tissue Adhesives snd Procedure Kits (sipas listes 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.