Verilux

GUDID 00817387026543

BEAR DOWN CONSULTING

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• Primary Device ID: 00817387026543
• NIH Device Record Key: ff8d1b86-7683-44cb-abff-be0766b3371c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Verilux
• Version Model Number: VT39WW1
• Company DUNS: 040869867
• Company Name: BEAR DOWN CONSULTING
• 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: false
• 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	00817387026543 [Primary]

FDA Product Code

• KZF: Device, Medical Examination, Ac 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: 2023-05-25
• Device Publish Date: 2023-05-17

On-Brand Devices [Verilux]

• 00768533140036: VT22WW3
• 00817387026765: VT53WW4
• 00768533140081: VT41WW3
• 00817387026543: VT39WW1
• 00817387025805: VT43CG3
• 00817387025799: VT43MB3
• 00817387024228: VT37WW1
• 00768533140104: VT52WW3
• 00768533140098: VT42WW3
• 00768533140067: VT43WW3
• 00768533140050: VT31WW3
• 00768533140043: VT32WW3