maxill Frames Eyewear Kids

GUDID D8926070553265D21

MAXILL, INC.

Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable Eye splash shield, reusable
Primary Device IDD8926070553265D21
NIH Device Record Key8d04b051-3a26-4a1a-8171-e73b11ee7a6a
Commercial Distribution StatusIn Commercial Distribution
Brand Namemaxill Frames Eyewear Kids
Version Model Number6070553265D2
Company DUNS079343581
Company NameMAXILL, 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
HIBCCD8926070553265D20 [Primary]
HIBCCD8926070553265D21 [Package]
Contains: D8926070553265D20
Package: Box [5 Units]
In Commercial Distribution
HIBCCD8926070553265D22 [Package]
Package: Case [50 Units]
In Commercial Distribution

FDA Product Code

HOYShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-22
Device Publish Date2022-11-14

On-Brand Devices [maxill Frames Eyewear Kids]

D8926070553265D316070553265D3
D8926070553265D216070553265D2

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