Pro tech ll

GUDID G51031730

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51031730
• NIH Device Record Key: 1c85dd68-e65d-45ba-9b2d-ca1567c3640b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pro tech ll
• Version Model Number: 3173
• 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	G51031730 [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: 2024-05-16
• Device Publish Date: 2024-05-08

On-Brand Devices [Pro tech ll]

• G51031730: 3173
• G51031690: 3169
• G51031660: 3166
• G51031800: 3180
• G51031820: 3182
• G51031810: 3181
• G51031790: 3179
• G51031760: 3176
• G51031670: 3167
• G51031640: 3164
• G51031750: 3175
• G51031650: 3165
• G5103169: 3169