PURE SUNLIGHT 1713 R 200W

GUDID G1503230076176

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G1503230076176
• NIH Device Record Key: ee44f7ef-84e7-4504-88a0-e16013fe925c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PURE SUNLIGHT 1713 R 200W
• Version Model Number: 3230076176 B
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G1503230076176 [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: 2026-01-15
• Device Publish Date: 2026-01-07

Devices Manufactured by Light Sources, Inc.

• G5103348 - RENUVATAN: 2026-01-19
• G5103349 - RENUVATAN: 2026-01-19
• G1503230076176 - PURE SUNLIGHT 1713 R 200W: 2026-01-15
• G1503230076176 - PURE SUNLIGHT 1713 R 200W: 2026-01-15
• G51010910 - BEACH SUN: 2025-12-22
• G51014170 - SIGNATURE SERIES: 2025-12-22
• G51027080 - RAVE: 2025-12-12
• G51032490 - REDSUN: 2025-12-11
• G51033470 - RADIANCE: 2025-11-28