SOLAR BRONZE

GUDID G5103141

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5103141
• NIH Device Record Key: 0d158fac-8026-49e9-98eb-893d956aad6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLAR BRONZE
• Version Model Number: 3141
• Company DUNS: 075058495
• Company Name: Light Sources, 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G5103141 [Primary]

FDA Product Code

• LEJ: Booth, Sun Tan

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: 2025-04-01
• Device Publish Date: 2025-03-24

On-Brand Devices [SOLAR BRONZE]

• G51031480: 3148
• G51031460: 3146
• G51031380: 3138
• G51031360: 3136
• G51031430: 3143
• G51031350: 3135
• G5103142: 3142
• G5103140: 3140
• G5103141: 3141
• G5103147: 3147