Reciproc®
by Maillefer Instruments Holding Sàrl 18 variants
Ref V040012025040Model 10147
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 | Number++J00310147EC +J003V0400120250401 | Date18 Sep 2025 | 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- Withdrawn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
- Reciproc NiTi Rotary Single-use Sterile
- Model / Reference
- 10147, V040012025040
- Primary DI / UDI-DI
- +J003V0400120250401
- Basic UDI-DI
- ++J00310147EC
- Unit of Use DI
- +J003V0400120250400
- EMDN Code
- Q010507 Endodontic instruments (canal enlargers, files, rasps, etc.), single-use
- Device Class
- Class IIa
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- CH-MF-000016301
- Authorised representative
- Dentsply DeTrey GmbH DE-AR-000005904
Other devices from Maillefer Instruments Holding Sàrl
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