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Ilo LED 50-Hd

by ILO electronic GmbH

Ref 862-2251Model 1Chip/LED Compact system

Ilo LED 50-Hd (862-2251) 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 04250369708161), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503697862P4 Basic UDI-DI 04250369708161UDI-DIDate20 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250369708161 UDI-DI Date22 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503697862P4 registered 20 May 2026 Active
  • FDA GUDID UDI-DI 04250369708161 listed 22 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250369708161
  2. Registered EUDAMED 42503697862P4

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
LED 50 Hd EUDAMED
Ilo GUDID
Generic name
Endoscopic video image processing/light source system
Device name
Endoscopic combi
Model / Ref / Catalog
1Chip/LED Compact system, 862-2251, LED 50-HD
Primary DI / UDI-DI
04250369708161
Basic UDI-DI
42503697862P4
Direct marketing DI
04250369708161
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

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
1Chip/LED Compact system
862-2251
GUDID
LED 50-HD
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 04250369708161: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Endoscope video cameraEndoscopic video image processing/light source system

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Properties

  • Sterilise before use YesEUDAMEDNoGUDID
  • Premarket exempt
  • Serial number
Other properties (22, all answered No)