ProSun

GUDID 00850090008093

PROSUN INTERNATIONAL, LLC

Ultraviolet tanning device

• Primary Device ID: 00850090008093
• NIH Device Record Key: 3a30e493-e5e3-4a09-894a-71e6e69433d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProSun
• Version Model Number: Model 32/1-P
• Company DUNS: 621545883
• Company Name: PROSUN INTERNATIONAL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850090008093 [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: 2018-12-03
• Device Publish Date: 2018-11-01

On-Brand Devices [ProSun]

• 00850090008215: Model 52X
• 00850090008208: Model 48V8-E
• 00850090008192: Model 48V8
• 00850090008185: Model 48V6
• 00850090008178: Model 42X
• 00850090008161: Model 42V6
• 00850090008154: Model 42V3
• 00850090008147: Model 38X
• 00850090008130: Model 36X-P
• 00850090008123: Model 36X
• 00850090008116: Model 36V
• 00850090008109: Model 32J
• 00850090008093: Model 32/1-P
• 00850090008086: Model 32/1
• 00850090008079: Model 32
• 00850090008062: Model 28
• 00850090008055: Model 24J
• 00850090008048: Model 24
• 00850090008031: Model 12