IsoLED Flex I LED Exam Light

GUDID 01816835024277

IsoLED Flex I LED Examination Light, Mobile Floor Stand

Medical Illumination International Inc.

Mobile examination/treatment room light

• Primary Device ID: 01816835024277
• NIH Device Record Key: 6d3b32ba-bd24-4fda-91c7-1d41dd8e251c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IsoLED Flex I LED Exam Light
• Version Model Number: IL-2381
• Company DUNS: 093357739
• Company Name: Medical Illumination International Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816835024278 [Primary]
GS1	01816835024277 [Package]; Contains: 00816835024278; Package: BOX [1 Units]; In Commercial Distribution

FDA Product Code

• KYT: Light, Examination, Medical, Battery Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-10
• Device Publish Date: 2023-10-02

On-Brand Devices [IsoLED Flex I LED Exam Light]

• 01816835024277: IsoLED Flex I LED Examination Light, Mobile Floor Stand
• 01816835024260: IsoLED Flex I LED Examination Light, Surgical Table Rail Mount
• 01816835024253: IsoLED Flex I LED Examination Light, Wall Mount