LUMEBOX

GUDID 00860008109217

Lumebox LLC

Blue/red/infrared phototherapy lamp

• Primary Device ID: 00860008109217
• NIH Device Record Key: 39ebcdd7-c397-4f10-ad77-93bb39d01a20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUMEBOX
• Version Model Number: LB-001A
• Company DUNS: 119062624
• Company Name: Lumebox LLC
• 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	00860008109217 [Primary]

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

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: 2023-08-30
• Device Publish Date: 2023-08-22