P Flex Ureteral Stent Both Ends Open BEML with Hydrophilic Coating
by Blue Neem Medical Devices Private Limited 12 variants
Ref BEUSB00801817
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 | Number8905080BUSH7E 08905080034070 | Date11 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- Withdrawn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
- Ureteral Stent
- Model / Reference
- BEUSB00801817
- Primary DI / UDI-DI
- 08905080034070
- Basic UDI-DI
- 8905080BUSH7E
- EMDN Code
- U020302 Double loop ureteral stents
- Device Class
- Class IIa
- EU market of registration
- Czechia
Manufacturer details
- EUDAMED SRN
- IN-MF-000021793
- Authorised representative
- Arazy Group (Ireland) Ltd. IE-AR-000000093
From the manufacturer
Manufacturer's product page: View Product >
Other devices from Blue Neem Medical Devices Private Limited
See all devices from Blue Neem Medical Devices Private Limited →
Properties
Other properties (11)
- 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