Philips Sonicare BreathRx

GUDID 00075020034243

Discus Dental, LLC

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