DEPUS Lumboperitoneal Shunt Lumbar Catheter Kit MEDIUM PRESSURE with Polyprolene Connector Decurve Adult Reservoir
by Desu Medi̇kal Ürünler Ve Tibbi̇ Ci̇hazlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 2 variants
Ref LPDP-M-LPACK-RDCA
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-08683955204109WQ D-08683955204109WQ | Date24 May 2023 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- DEPUS Lumboperitoneal Shunt Lumbar Catheter Kit MEDIUM PRESSURE with Polyprolene Connector Decurve Adult Reservoir
- Model / Reference
- LPDP-M-LPACK-RDCA
- Primary DI / UDI-DI
- D-08683955204109WQ
- Basic UDI-DI
- B-08683955204109WQ
- EMDN Code
- N020301 Lumbo-peritoneal shunts
- Device Class
- Class III
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000031476
Other devices from Desu Medi̇kal Ürünler Ve Tibbi̇ Ci̇hazlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
Properties
Other properties (9)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No