INSTRUMENTS - Disc Hernia Forceps
Ref NRD-180-4-S
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number37004822INSTRUMENT138U 03700482266303 | Date4 Nov 2026 | StatusActive |
Official records
- EUDAMED public site 37004822INSTRUMENT138U
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- Withdrawn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
- INSTRUMENTS - Disc Hernia Forceps
- Model / reference
- NRD-180-4-S
- Primary DI / UDI-DI
- 03700482266303
- Basic UDI-DI
- 37004822INSTRUMENT138U
- Direct marketing DI
- 03700482266303
- EMDN code
- L110601 Disc hernia forceps, reusable
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000007304
Other devices from NovaSpine
Properties
Other properties (12)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No