BRILLIANCE ACTIVE BRONZER

GUDID G51029210

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51029210
• NIH Device Record Key: fa7a1464-6f8c-458b-8bfc-a15f06cbed71
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRILLIANCE ACTIVE BRONZER
• Version Model Number: 2921
• 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: true
• 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	G51029210 [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: 2024-06-13
• Device Publish Date: 2024-06-05

On-Brand Devices [BRILLIANCE ACTIVE BRONZER]

• G510196801: 1968
• G51028250: 2825
• G51024110: 2411
• G51029210: 2921
• G51019660: 1966
• G5101970: 1970
• G51033150: 3315