11894CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts
Albania medical device registration · Medtronic Inc. 710 Medtronic Parkway Minneapolis MN 55432 USA · III · Model CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts (Sipas listes bashkengjitur) · Registered April 29, 2022
- Risk Class
- III
- Product Model
- CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts (Sipas listes bashkengjitur)
- Product Name
- CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts
- Registration Date
- April 29, 2022
- Analysis ID
- 11894
Kateter dhe shunte lumboperitoneale qe perdoren ne neurokirurgji.
Access comprehensive regulatory information for CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts in the Albania medical device market through Pure Global AI's free database. This III medical device is manufactured by Medtronic Inc. 710 Medtronic Parkway Minneapolis MN 55432 USA. The device was registered on April 29, 2022.
This page provides complete registration details including product model (CSF-Lumboperitoneal Catheters :CSF-Lumboperitoneal shunts (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.