BM Urethral Dilators
by Bonree Medical Co., Ltd. 15 variants
Ref 404 20 22 2Model 8FR, 10FR, 12FR, 14FR, 16FR, 18FR, 20Fr, 22Fr, 24Fr, 26Fr
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 | Number697209192UHD39L6 06942382609690 | Date1 Jun 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- Withdrawn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
- Device Name
- Urethral Dilators
- Model / Reference
- 8FR, 10FR, 12FR, 14FR, 16FR, 18FR, 20Fr, 22Fr, 24Fr, 26Fr, 404 20 22 2
- Primary DI / UDI-DI
- 06942382609690
- Basic UDI-DI
- 697209192UHD39L6
- Direct Marketing DI
- 06942382609690
- EMDN Code
- U03010201 Urethral dilators
- 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