PROTECH II

GUDID G51032030

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51032030
• NIH Device Record Key: bdc599ed-914f-4263-97e4-54dd9f23bbf4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROTECH II
• Version Model Number: 3203
• 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	G51032030 [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: 2025-03-12
• Device Publish Date: 2025-03-04

On-Brand Devices [PROTECH II]

• G51031700: 3170
• G5103177: 3177
• G51031680: 3168
• G51032030: 3203
• G51032020: 3202
• G51031720: 3172