MERIDIAN BRONZER

GUDID G51008110

Light Sources, Inc.

Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device Ultraviolet tanning device

• Primary Device ID: G51008110
• NIH Device Record Key: cf2c6896-9739-4784-b33d-016be21bf808
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MERIDIAN BRONZER
• Version Model Number: 0811
• 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	G51008110 [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: 2024-07-04
• Device Publish Date: 2024-06-26

On-Brand Devices [MERIDIAN BRONZER]

• G51014260: 1426
• G51008110: 0811