Philips Zoom

GUDID 08710103632092

Discus Dental, LLC

Dental cheek retractor, professional, single-use
Primary Device ID08710103632092
NIH Device Record Key5091add2-867f-499c-8ded-02dad1e62546
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips Zoom
Version Model NumberDIS574/01
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-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108710103632092 [Primary]

FDA Product Code

EIFACCESSORIES, RETRACTOR, DENTAL

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 Zoom]

08710103632092DIS574/01
08710103632085DIS573/01
00075020044129DIS716/01
08710103632122DIS578/01
00075020035011DIS558/01
08710103611967DIS203/30

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