Ilo

FDA UDI

Class I (US FDA UDI)

by ILO electronic GmbH

Identity

Trade Name: ILO FDA UDI
Generic Name: Endoscope video camera FDA UDI
Device Name: Camera head for 1MOS HD video imaging system FDA UDI
Model / Reference: Camera head LED50-HDII FDA UDI
Description: Camera head for 1MOS HD video imaging system FDA UDI

Identifiers

Catalog Number: 740-2021 FDA UDI
Primary DI / UDI-DI: 04250369709779 FDA UDI
FDA Product Code: KQM FDA UDI
GMDN Term: Endoscope video camera 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Endoscope video camera

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: ILO electronic GmbH

Sources (1)

FDA UDI ea2e7e1d-811a-440a-851a-bc1485c93c02 35 fields · synced May 30, 2026