iLux LF D20 1LFD20
Ref 10LFD20
iLux LF D20 1LFD20 is a musculoskeletal/physical therapy laser (EU MDD Class IIb; FDA Class II; FDA product code ILY, Lamp, Infrared, Therapeutic Heating) made by Mectronic Medicale SRL, registered in EUDAMED on 13 May 2026 (Basic UDI-DI B-08051499974091) and listed in FDA GUDID since 10 Oct 2024 (UDI-DI 08051499974091), active as of 23 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-08051499974091 08051499974091 | Date13 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08051499974091 | Date10 Oct 2024 | StatusListed |
Official records
- EUDAMED public site B-08051499974091
- AccessGUDID record 08051499974091
Across registries
- EUDAMED Basic UDI-DI B-08051499974091 registered 13 May 2026 Active
- FDA GUDID UDI-DI 08051499974091 listed 10 Oct 2024 Listed
Timeline
- Listed FDA GUDID 08051499974091
- Registered EUDAMED B-08051499974091
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- ILUX SMART (20W 810+980nm) EUDAMEDiLux LF D20 GUDID
- Generic name
- Musculoskeletal/physical therapy laser, professional
- Model / reference
- 10LFD20 EUDAMED1LFD20 GUDID
- Primary DI / UDI-DI
- 08051499974091
- Basic UDI-DI
- B-08051499974091
- FDA product code
- ILY
- EMDN code
- Z120615 Therapeutic lasers
- GMDN term
- Musculoskeletal/physical therapy laser, professional
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 890.5500
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10LFD20 | 1LFD20 |
| Device class | Class IIb | Class II |
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