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Ilo

FDA UDI

Class I (US FDA UDI)

by ILO electronic GmbH

Identity

Trade Name
ILO FDA UDI
Generic Name
Endoscopic video image processing/light source system FDA UDI
Device Name
1MOS HD video imaging system FDA UDI
Model / Reference
LED 50-HD-USB FDA UDI
Description
1MOS HD video imaging system FDA UDI

Identifiers

Catalog Number
862-2201 FDA UDI
Primary DI / UDI-DI
04250369708178 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Endoscopic video image processing/light source system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Ilo by ILO electronic GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing/light source system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ILO electronic GmbH

Sources (1)

  • FDA UDI 80873adc-4967-4faf-9334-3c0008004333 35 fields · synced May 30, 2026