Prophy Paste

GUDID 00190707007522

Prophy Paste Nonfluoride

ORTHO ORGANIZERS, INC.

Dentifrice

• Primary Device ID: 00190707007522
• NIH Device Record Key: e95059d7-9dfd-4d96-b88d-e58a943dfc6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prophy Paste
• Version Model Number: 504-90
• Company DUNS: 062165188
• Company Name: ORTHO ORGANIZERS, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190707007522 [Primary]

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-08

On-Brand Devices [Prophy Paste]

• 00190707007546: Prophy Paste Nonfluoride
• 00190707007522: Prophy Paste Nonfluoride