Sensor RXS 1000
by Rolence Enterprise Inc. EUDAMED510(k)
Active
Ref 1501Model RXS 1000
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-04713909450635 | Date1 Dec 2022 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK202369 | Date15 Sep 2021 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- United States
- European Union
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 25 Oct 2026.
Specification
- Device Name
- Intraoral Digital X-Ray Sensor
- Model / Reference
- RXS 1000, 1501
- Primary DI / UDI-DI
- 04713909450635
- Basic UDI-DI
- B-04713909450635
- EMDN Code
- Z11039016 Mobile radiographic units
- Device Class
- Class IIb
- Market of Registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TW-MF-000024483
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Rolence Enterprise Inc.
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No