Waterpik Prophy Paste

GUDID D686200334973

PROPHY PASTE (MELON) (COARSE) (200PK)

WATER PIK, INC.

Dentifrice

• Primary Device ID: D686200334973
• NIH Device Record Key: 7e14e642-9973-4d45-af52-4ba8191d4222
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Waterpik Prophy Paste
• Version Model Number: 20033497
• Company DUNS: 001804074
• Company Name: WATER PIK, 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D686200334970 [Primary]
HIBCC	D686200334973 [Unit of Use]

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: 2025-01-20
• Device Publish Date: 2025-01-10

On-Brand Devices [ Waterpik Prophy Paste]

• D686200334973: PROPHY PASTE (MELON) (COARSE) (200PK)
• D686200334963: PROPHY PASTE (MELON) (MEDIUM) (200PK)