Philips Zoom

GUDID 08710103611967

Discus Dental, LLC

Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles Radiation shielding goggles/spectacles
Primary Device ID08710103611967
NIH Device Record Keya81e47a0-60f2-4121-8fa4-6dae81113144
Commercial Distribution Discontinuation2024-01-31
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips Zoom
Version Model NumberDIS203/30
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
GS108710103611967 [Primary]

FDA Product Code

IWSShield, eye, radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-01-30
Device Publish Date2020-09-20

On-Brand Devices [Philips Zoom]

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

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