PROPHY PASTE

GUDID D89260705405502

MAXILL, INC.

Dentifrice

• Primary Device ID: D89260705405502
• NIH Device Record Key: e720cfef-f468-43fb-a9ab-75d8c6e1bcbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROPHY PASTE
• Version Model Number: 6070540550
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 200
• 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: 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
HIBCC	D89260705405500 [Unit of Use]
HIBCC	D89260705405501 [Primary]
HIBCC	D89260705405502 [Package]; Contains: D89260705405501; Package: Case [4000 Units]; In Commercial Distribution

FDA Product Code

• EJR: Agent, Polishing, Abrasive, Oral 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: 2022-10-28
• Device Publish Date: 2022-10-20

On-Brand Devices [PROPHY PASTE]

• D89260705405852: 6070540585
• D89260705405812: 6070540581
• D89260705405762: 6070540576
• D89260705405752: 6070540575
• D89260705405722: 6070540572
• D89260705405712: 6070540571
• D89260705405662: 6070540566
• D89260705405652: 6070540565
• D89260705405622: 6070540562
• D89260705405612: 6070540561
• D89260705405602: 6070540560
• D89260705405502: 6070540550