Desu
by Desu Medi̇kal Ürünler Ve Tibbi̇ Ci̇hazlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 1,000+ variants
Ref ALPDP-L-LTCK-RDFR
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-8683955201771DP | Date5 Nov 2025 | 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- Withdrawn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 QUICK RESPONSE Lumboperitoneal Yetişkin Şant, Lomber Kateter Kit Titanyum Konnektör Defit Yetişkin Rezervuar ile DÜŞÜK BASINÇ
- Model / Reference
- ALPDP-L-LTCK-RDFR
- Primary DI / UDI-DI
- D-8683955201771DP, D-8680454756221AF
- Basic UDI-DI
- B-8683955201771DP, B-8680454756221AF
- 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 (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No