optiprint lumina
by dentona AG EUDAMEDGUDID
Active
Ref 48288
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number04260670160947 | Date29 Jun 2026 | StatusIn distribution |
| European Union | CE/MDD EUDAMED | NumberB-04260670160947 | Date20 Jan 2026 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Generic Name
- Dental appliance fabrication material, resin
- Model / Reference
- 48288
- Primary DI / UDI-DI
- 04260670160947
- Basic UDI-DI
- B-04260670160947
- FDA Product Code
- ELK
- EMDN Code
- Q010699 Materials for the preparation of custom-made dental devices - other
- GMDN Term
- Dental appliance fabrication material, resin
- Device Class
- Class IIa EUDAMEDClass I GUDID
- Regulation Number
- 872.3910
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class I |
Manufacturer details
- EUDAMED SRN
- DE-MF-000005550
Other devices from dentona AG
Properties
Other properties (16)
- 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No