Creative Group Enterprise Inc

GUDID 00876008005800

Creative Group Enterprise, Inc

Magnifying spectacles
Primary Device ID00876008005800
NIH Device Record Key4a84d753-3184-4209-aa7f-f02cb391dfee
Commercial Distribution StatusIn Commercial Distribution
Brand NameCreative Group Enterprise Inc
Version Model NumberR Eyewear
Company DUNS117225686
Company NameCreative Group Enterprise, 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
GS100876008005800 [Primary]

FDA Product Code

HOISpectacle, Magnifying

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-24
Device Publish Date2022-11-16

On-Brand Devices [Creative Group Enterprise Inc]

00876008005817S Eyewear
00876008005800R Eyewear

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