Ilo LED 50-Hd-Usb
Ref 862-2201Model 1Chip/LED Compact system
Ilo LED 50-Hd-Usb (862-2201) is a Class I device made by ILO electronic GmbH, registered in EUDAMED on 20 May 2026 (Basic UDI-DI 42503697862P4) and listed in FDA GUDID since 22 Jun 2023 (UDI-DI 04250369708178), active as of 23 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number42503697862P4 04250369708178 | Date20 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250369708178 | Date22 Jun 2023 | StatusListed |
Official records
- EUDAMED public site 42503697862P4
- AccessGUDID record 04250369708178
Across registries
- EUDAMED Basic UDI-DI 42503697862P4 registered 20 May 2026 Active
- FDA GUDID UDI-DI 04250369708178 listed 22 Jun 2023 Listed
Timeline
- Listed FDA GUDID 04250369708178
- Registered EUDAMED 42503697862P4
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- LED 50 Hd USB EUDAMEDIlo GUDID
- Generic name
- Endoscopic video image processing/light source system
- Device name
- Endoscopic combi
- Model / Ref / Catalog
- 1Chip/LED Compact system, 862-2201, LED 50-HD-USB
- Primary DI / UDI-DI
- 04250369708178
- Basic UDI-DI
- 42503697862P4
- Direct marketing DI
- 04250369708178
- FDA product code
- KQM
- EMDN code
- Z12020405 Surgical cameras
- GMDN term
- Endoscopic video image processing/light source system
- Device class
- Class I
- Regulation number
- 878.4160
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 1Chip/LED Compact system 862-2201 | LED 50-HD-USB |
| Sterilise before use | Yes | No |