Single-use Snare Probe
by Leo Medical Co., Ltd. 3 variants
Ref L17NA251825F, L17NA252410F, L17NA251815FModel L17NA251810F
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 | Number69236465L17Z5 | Date17 Dec 2024 | 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- Withdrawn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
- Device Name
- Single-use Snare Probe
- Model / Reference
- L17NA251810F, L17NA251825F, L17NA252410F, L17NA251815F
- Primary DI / UDI-DI
- 06923646517678, 06923646517739, 06923646517661, 06923646517654
- Basic UDI-DI
- 69236465L17Z5
- Direct Marketing DI
- 06923646517678069236465177390692364651766106923646517654
- EMDN Code
- G03030101 Polypectomy snares, revolving
- Device Class
- Class IIb
- EU market of registration
- PolandItaly
Manufacturer details
- EUDAMED SRN
- CN-MF-000012017
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Leo Medical Co., Ltd.
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