CariFree

GUDID 00856596006151

A mixture of 5% sodium fluoride in a resin carrier, packaged in a convenient single-use dose for easy application

Dental Alliance Holdings LLC

Dental cavity varnish

• Primary Device ID: 00856596006151
• NIH Device Record Key: c9ad39c4-afe8-47e7-90a2-60da69fdf276
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CariFree
• Version Model Number: Raspberry
• Company DUNS: 195544965
• Company Name: Dental Alliance Holdings 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856596006151 [Primary]

FDA Product Code

• LBH: Varnish, Cavity

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: 2023-02-23
• Device Publish Date: 2023-02-15

On-Brand Devices [CariFree]

• 00856596006168: A mixture of 5% sodium fluoride in a resin carrier, packaged in a convenient single-use dose for
• 00856596006151: A mixture of 5% sodium fluoride in a resin carrier, packaged in a convenient single-use dose for