BM Ureteral Stent Sets
by Bonree Medical Co., Ltd. 12 variants
Ref 321 40 18 2Model 4.0FR, 4.7FR, 5.0FR, 6.0FR, 7.0FR, 8.0FR
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 | Number697209192USS25QK 06942382609874 | Date10 Oct 2025 | 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- Withdrawn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
- Ureteral Stent Sets
- Model / Reference
- 4.0FR, 4.7FR, 5.0FR, 6.0FR, 7.0FR, 8.0FR, 321 40 18 2
- Primary DI / UDI-DI
- 06942382609874
- Basic UDI-DI
- 697209192USS25QK
- Direct Marketing DI
- 06942382609874
- EMDN Code
- U020302 Double loop ureteral stents
- Device Class
- Class IIa
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- CN-MF-000017844
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Bonree 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