PROTECH

GUDID G51028810

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51028810
• NIH Device Record Key: dffd8dc0-f9ab-401b-aacd-89a6f8f29d2d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROTECH
• Version Model Number: 2881
• 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	G51028810 [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: 2025-03-12
• Device Publish Date: 2025-03-04

Devices Manufactured by Light Sources, Inc.

• G5100717 - AURORA TANNING SYSTEM: 2025-06-05
• G5102225 - SUN ANGEL: 2025-06-05
• G51007420 - EQUATOR SUN: 2025-05-22
• G51030080 - SUNANGEL: 2025-05-22
• G51022410 - BRILLIANCE BRONZER: 2025-05-20
• G5101219 - GENESIS: 2025-05-14
• G51024570 - UV POWER: 2025-05-14
• G51031540 - REJUVENESSENCE: 2025-05-14