LUMINANT

GUDID 00049696736701

LUMINANT BO TB W/REMOVEABLE HD

FOURSTAR GROUP INC.

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• Primary Device ID: 00049696736701
• NIH Device Record Key: f1ef23e0-53ff-442e-9547-7dcd1c8e8f44
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUMINANT
• Version Model Number: 11012436DA
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049696736701 [Primary]

FDA Product Code

• JEQ: Toothbrush, Powered

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: 2023-02-13
• Device Publish Date: 2023-02-05

On-Brand Devices [LUMINANT]

• 00049696736701: LUMINANT BO TB W/REMOVEABLE HD
• 00049696880145: MINI TRAVEL B/O TOOTHBRUSH
• 00049696509688: LUMINANT ORAL CARE KIT 4PC
• 00049696186889: DUAL ACTION POWERBRUSH
• 00049696511735: MP LUMINANT POWER TOOTHBRUSH