FRITZ EYEWEAR

GUDID 08012794011737

SPECTACLE FRAME WITH DEMOLENSES

LA GIARDINIERA SRL

Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame Spectacle frame
Primary Device ID08012794011737
NIH Device Record Keyec6a4f87-859c-4127-8bf4-3b41fa0d064d
Commercial Distribution StatusIn Commercial Distribution
Brand NameFRITZ EYEWEAR
Version Model NumberSPECTACLE FRAME
Company DUNS428689665
Company NameLA GIARDINIERA SRL
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
GS108012794011737 [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 Date2023-10-04
Device Publish Date2023-09-26

On-Brand Devices [FRITZ EYEWEAR]

08012794011737SPECTACLE FRAME WITH DEMOLENSES
08012794011720PLASTIC FRAME WITH SUNLENSES

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.