Fascial Dilator
by Blue Neem Medical Devices Private Limited 19 variants
Ref BFDN0080200S
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 | Number8905080BPDGH 08905080000693 | Date21 Apr 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- Withdrawn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
- Percutaneous Dilators
- Model / Reference
- BFDN0080200S
- Primary DI / UDI-DI
- 08905080000693
- Basic UDI-DI
- 8905080BPDGH
- EMDN Code
- U03010199 Percutaneous nephrostomy, sequential dilators - other
- 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 (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