RAVE

GUDID G51018250

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51018250
• NIH Device Record Key: f8601abc-23f7-46c4-8e38-482aa98947b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAVE
• Version Model Number: 1825
• 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	G51018250 [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: 2024-12-11
• Device Publish Date: 2024-12-03

On-Brand Devices [RAVE]

• G51028710: 2871
• G51018260: 1826
• G51018490: 1849
• G51027540: 2754
• G51018270: 1827
• G510269701: 2697
• G51018350: 1835
• G51018340: 1834
• G51018320: 1832
• G51018290: 1829
• G51026810: 2681
• G510198904: 1989
• G51018390: 1839
• G51018750: 1875
• G51018370: 1837
• G51018280: 1828
• G510189904: 1899
• G51018740: 1874
• G51018410: 1841
• G510RAVE0: 1830
• G51026220: 2622
• G51018760: 1876
• G5102699: 2699
• G5102758: 2758
• G51018330: 1833
• G51018430: 1843
• G51018250: 1825