Liceguard

GUDID 00663580000800

Liceguard, LLC

Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit Lice removal/prevention kit

• Primary Device ID: 00663580000800
• NIH Device Record Key: f7e491c1-d68e-4d20-bbb6-f31b889166b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liceguard
• Version Model Number: No Nit Kit
• Company DUNS: 079196902
• Company Name: Liceguard, LLC
• 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: false
• Serial Number: false
• Manufacturing Date: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00663580000800 [Primary]

FDA Product Code

• PUN: Lice Removal Kit Containing A Solution

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: 2023-08-28
• Device Publish Date: 2023-08-18

On-Brand Devices [Liceguard]

• 00663580012025: RobiComb Pro
• 00663580009209: Egg & Lice Combing Kit
• 00663580000800: No Nit Kit
• 00663580000022: RobiComb