PURE SUNLIGHT

GUDID G5103230

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5103230
• NIH Device Record Key: 1772e287-f6a8-4280-9dea-848cb741529b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PURE SUNLIGHT
• Version Model Number: 3230074860
• 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	G5103230 [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: 2024-10-02
• Device Publish Date: 2024-09-24

Devices Manufactured by Light Sources, Inc.

• G5101390 - SIGNATURE SERIES: 2024-10-14
• G51020420 - HEX TRU TAN: 2024-10-14
• G5103239 - HEX SMART: 2024-10-14
• G5102872 - RAVE RUSH: 2024-10-11
• G5100709 - MIDDAY SUN: 2024-10-07
• G5100734 - NEVADA SUN: 2024-10-07
• G5102956 - BRILLIANCE ADVANCED ACTIVE BRONZER: 2024-10-07
• G5103230 - PURE SUNLIGHT: 2024-10-02
• G5103230 - PURE SUNLIGHT: 2024-10-02