SUN MASTER

GUDID G51021370

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51021370
• NIH Device Record Key: 197f9284-1af6-49d2-b69f-1cc7c2c92942
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUN MASTER
• Version Model Number: 2137
• 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	G51021370 [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: 2024-05-17
• Device Publish Date: 2024-05-09

On-Brand Devices [SUN MASTER]

• G51021560: SUNMASTER CLEARTECH 20 F71/HO/BP/ SOL65 GR
• G51024860: 2486
• G51024850: 2485
• G51021370: 2137
• G51021350: 2135
• G51019600: 1960
• G51019590: 1959