ProFlare

GUDID 00348783004564

ProFlare Articulating Disposable Prophy Angle Sample

PREMIER DENTAL PRODUCTS COMPANY

Dentifrice

• Primary Device ID: 00348783004564
• NIH Device Record Key: 4f0d16fa-6180-4ec5-befe-cfb6d69cb9a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProFlare
• Version Model Number: 5500193
• Company DUNS: 014789663
• Company Name: PREMIER DENTAL PRODUCTS COMPANY
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00348783004564 [Primary]

FDA Product Code

• EHK: Cup, Prophylaxis

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: 2023-11-03
• Device Publish Date: 2023-10-26

On-Brand Devices [ProFlare]

• 00348783004564: ProFlare Articulating Disposable Prophy Angle Sample
• 00348783001181: ProFlare Articulating DPA (Bag of 125)