EYEVAN7285

GUDID 04571445037679

EYEVAN INC.

Spectacle frame
Primary Device ID04571445037679
NIH Device Record Keyed6191b3-0a28-4c4d-a2c2-588650f1c465
Commercial Distribution StatusIn Commercial Distribution
Brand NameEYEVAN7285
Version Model Number156I-B 45 332800
Company DUNS705184505
Company NameEYEVAN INC.
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 Batchfalse
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
GS104571445037679 [Primary]

FDA Product Code

HQZFrame, Spectacle

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-06-26
Device Publish Date2023-01-01

On-Brand Devices [EYEVAN7285]

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04582667989400177 46 801
04582667989394177 46 800
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04582667985709171 48 817
04582667985693171 48 805
04582667985686170 49 901-G DK.G15
04582667985679170 49 900-G DK.BLU
04582667985662170 49 805-G LT.GRY
04582667985655170 49 801-G GRY
04582667985648170 49 800-G DK.BR
04582667984108163(48)RX 48 901
04582667984092163(48)RX 48 900
04582667984085163(48)RX 48 801
04582667984078163(48)RX 48 800
04582667982746169 46 901
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04582667982722169 46 815
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04582667982463167 45 913
04582667982456167 45 901
04582667982449167 45 900
04582667982432167 45 800
04582667979906156 46 913
04582667979890156 46 805
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