EYEVAN7285

GUDID 04582669019402

EYEVAN INC.

Spectacle frame
Primary Device ID04582669019402
NIH Device Record Key61799be0-6ada-4b00-bf48-2e2ed842ec73
Commercial Distribution StatusIn Commercial Distribution
Brand NameEYEVAN7285
Version Model Number340MR(46)E 46 351
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
GS104582669019402 [Primary]

FDA Product Code

HQZFrame, Spectacle

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-08
Device Publish Date2024-10-31

On-Brand Devices [EYEVAN7285]

04582667989431177 46 901
04582667989424177 46 900
04582667989400177 46 801
04582667989394177 46 800
04582667985822176 47 902
04582667985815176 47 900
04582667985808176 47 801
04582667985792176 47 800
04582667985747172 47 901
04582667985730172 47 817
04582667985723171 48 901
04582667985716171 48 920
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
04582667982739169 46 900
04582667982722169 46 815
04582667982715169 46 800
04582667982708166E 46 802902
04582667982692166E 46 802800
04582667982685166E 46 900
04582667982678166E 46 800
04582667982654166 46 802800
04582667982647166 46 900
04582667982630166 46 800
04582667982609165E 45 815
04582667982593165E 45 800
04582667982586165 45 901
04582667982579165 45 900
04582667982562165 45 815
04582667982555165 45 800
04582667982500168 47 901
04582667982494168 47 900
04582667982487168 47 817
04582667982470168 47 805
04582667982463167 45 913
04582667982456167 45 901
04582667982449167 45 900
04582667982432167 45 800
04582667979906156 46 913
04582667979890156 46 805
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.