LiNA MaxFlow EndoHook
Ref SIP-005-L-8, 908-N, 908-L, 908-SModel SIP-005-L-4, SIP-005-L-8, 908-L, 908-N, 908-S, 308-L, 308-L-400, 308-S, 308-N
Active
CE MDR
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/MDR | Number57082651010-2YV | Date23 Jan 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Trade Name
- LiNA MaxFlow EndoHookLiNA EndoHook
- Model / Reference
- SIP-005-L-4, SIP-005-L-8, 908-L, 908-N, 908-S, 308-L, 308-L-400, 308-S, 308-N
- Primary DI / UDI-DI
- 05708265016105, 05708265015412, 05708265015399, 05708265015436
- Basic UDI-DI
- 57082651010-2YV, 57082651005-1ZD
- EMDN Code
- K02010199, K020199
- Device Class
- Class IIb
- EU market of registration
- Denmark
Manufacturer details
- EUDAMED SRN
- CH-MF-000046832
- Authorised representative
- LiNA Medical Polska Sp. z o.o. PL-AR-000039364
Other devices from LiNA Medical AG
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No