Disposable Hybrid Polypectomy Snare
by Yangzhou Fartley Medical Instrument Technology Co., Ltd. 64 variants
Ref FTL-PSH-24-230-15-R-25-O
Active
CE MDR 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number697090085100987 06936603233658 | Date25 Mar 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK220790 | Date27 Jun 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 24 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Device Name
- Disposable Polypectomy Hybrid Snares
- Model / Reference
- FTL-PSH-24-230-15-R-25-O
- Primary DI / UDI-DI
- 06936603233658
- Basic UDI-DI
- 697090085100987
- Direct Marketing DI
- 06936603233658
- EMDN Code
- G03030199 Polypectomy snares - other
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000009371
- Authorised representative
- Prolinx GmbH DE-AR-000005129
Other devices from Yangzhou Fartley Medical Instrument Technology Co., Ltd
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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