ILO LED50-EcoHD II

by ILO electronic GmbH

ILO LED50-EcoHD II (862-2501) is a Class I device made by ILO electronic GmbH, listed in FDA GUDID since 22 Jun 2023 (UDI-DI 04250369709021), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04250369709021 UDI-DI	Date22 Jun 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04250369709021

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Ilo
Generic name: Endoscopic video image processing/light source system
Model / Ref / Catalog: LED50-EcoHD II, 862-2501

Primary DI / UDI-DI: 04250369709021
FDA product code: KQM
GMDN term: Endoscopic video image processing/light source system

Device class: Class I
Regulation number: 878.4160
GUDID distribution status: In Commercial Distribution

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Properties

Premarket exempt
Serial number

Other properties (13, all answered No)