EndoPilot comfort
Ref 110 0101
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 | Number426048299M11066 | Date11 Mar 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK202906 | Date13 Apr 2021 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 25 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Device Name
- EndoPilot
- Model / Reference
- 110 0101
- Primary DI / UDI-DI
- 04260482990688, 04260482990619
- Basic UDI-DI
- 426048299M11066, B-04260482990619
- EMDN Code
- Q010199 Conservative dentistry and endodontics devices - other
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005266
Other devices from Schlumbohm GmbH & Co. KG
Properties
Other properties (13)
- Sterile: No
- 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