GENESIS

GUDID G51031870

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51031870
• NIH Device Record Key: 0feead99-2905-4984-95f0-23e73a176e7a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GENESIS
• Version Model Number: 3187
• 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	G51031870 [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: 2024-12-10
• Device Publish Date: 2024-12-02

On-Brand Devices [GENESIS]

• G51031560: 3156
• G51031900: 3190
• G51026520: 2652
• G51032410: 3241
• G51030940: 3094
• G51030460: 3046
• G51011850: 1185
• G51030450: 3045
• G51031980: 3198
• G51031890: 3189
• G51031620: 3162
• G51031580: 3158
• G51031570: 3157
• G51024840: 2484
• G51011660: 1166
• G51030930: 3093
• G51032200: 3220
• G51032000: 3200
• G51031990: 3199
• G51031600: 3160
• G51031590: 3159
• G51030300: 3030
• G51025630: 2563
• G51014000: 1400
• G51025600: 2560
• G51011890: 1189
• G51030800: 3080
• G51027720: 2772
• G51012870: 1287
• G51026590: 2659
• G51010320: 1032
• G51014460: 1446
• G51025610: 2561
• G51025470: 2547
• G51032530: 3253
• G51032250: 3225
• G51032240: 3224
• G51032010: 3201
• G51021330: 2133
• G51022390: FR71T12/BL/VHO/BP/3.5/230 160W
• G51031880: 3188
• G51031870: 3187
• G5103046: 3046