UROMED HEPARIUS Ureteral Stent
by UROMED Kurt Drews KG 48 variants
Ref 4155.30
Active
CE MDR
Valid until
23 Jul 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number04250098810055ET 04250098841184 | Date3 Feb 2026 | StatusActive |
Certificates
- 20561GB450250724 Active
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 24 Jul 2025
- Expires
- 23 Jul 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- US01
- Model / Reference
- 4155.30
- Primary DI / UDI-DI
- 04250098841184
- Basic UDI-DI
- 04250098810055ET
- EMDN Code
- U020302 Double loop ureteral stents
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000006084
Other devices from UROMED Kurt Drews KG
Properties
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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