SAF (self-adjusting file)
by ReDent Nova GmbH & Co. KG 8 variants
Ref SF-10-200-031-0062Model SAF
Active
CE MDR 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number426235751SAF0012C 14262357510059 | Date31 Mar 2025 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK092933 | Date14 Jan 2010 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 24 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Model / Reference
- SAF, SF-10-200-031-0062
- Primary DI / UDI-DI
- 14262357510059
- Basic UDI-DI
- 426235751SAF0012C
- Direct Marketing DI
- 14262357510059
- EMDN Code
- Q010507 Endodontic instruments (canal enlargers, files, rasps, etc.), single-use
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000032545
Other devices from ReDent Nova GmbH & Co. KG
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