maxill Frames Eyewear

GUDID D89260705532631

MAXILL, INC.

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Primary Device ID	D89260705532631
NIH Device Record Key	5bf53281-16b9-4340-b3c9-08f1edf3c290
Commercial Distribution Status	In Commercial Distribution
Brand Name	maxill Frames Eyewear
Version Model Number	6070553263
Company DUNS	079343581
Company Name	MAXILL, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D89260705532630 [Primary]
HIBCC	D89260705532631 [Package] Contains: D89260705532630 Package: Box [5 Units] In Commercial Distribution
HIBCC	D89260705532632 [Package] Package: Case [50 Units] In Commercial Distribution

FDA Product Code

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

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2022-11-22
Device Publish Date	2022-11-14

On-Brand Devices [maxill Frames Eyewear]

D89260705532631	6070553263
D89260705532601	6070553260