Philips Sonicare BreathRx

GUDID 00075020034243

Discus Dental, LLC

Tongue scraper, reusable
Primary Device ID00075020034243
NIH Device Record Keya3fa2b1c-2981-41ad-84f7-36942ad925d2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips Sonicare BreathRx
Version Model NumberDIS442/02
Company DUNS831726109
Company NameDiscus Dental, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100075020034243 [Primary]

FDA Product Code

LCNSCRAPER, TONGUE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-07
Device Publish Date2020-08-28

On-Brand Devices [Philips Sonicare BreathRx]

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

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