Philips Sonicare BreathRx

GUDID 00075020034243

Discus Dental, LLC

Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable Tongue scraper, reusable

• Primary Device ID: 00075020034243
• NIH Device Record Key: a3fa2b1c-2981-41ad-84f7-36942ad925d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Sonicare BreathRx
• Version Model Number: DIS442/02
• Company DUNS: 831726109
• Company Name: Discus Dental, LLC
• 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: false
• Lot Batch: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00075020034243 [Primary]

FDA Product Code

• LCN: SCRAPER, TONGUE

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: 2020-09-07
• Device Publish Date: 2020-08-28

On-Brand Devices [Philips Sonicare BreathRx]

• 00075020049445: DIS350/11
• 00075020049421: DIS251/11
• 00075020048066: DIS359/11
• 00075020048059: DIS359/03
• 00075020048042: DIS357/11
• 00075020048035: DIS357/03
• 00075020048004: DIS251/01
• 00075020034243: DIS442/02
• 00075020034236: DIS442/01