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Ilo LED50-Hd II Rw Us

by ILO electronic GmbH

Ilo LED50-Hd II Rw Us (862-2519) is a Class I device made by ILO electronic GmbH, listed in FDA GUDID since 9 Sep 2024 (UDI-DI 04250369709762), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250369709762 UDI-DI Date9 Sep 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • 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  • Withdrawn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-HD II RW US, 862-2519
Primary DI / UDI-DI
04250369709762
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

Related devices

Category: Endoscopic video image processing/light source system

Similar devices in this category

Other devices filed under Endoscopic video image processing/light source system.

Other devices from ILO electronic GmbH

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Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)