Catalog Number

-

Brand Name

DISNEY

Version/Model Number

10251901.FMY

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HQY

Product Code Name

Sunglasses (non-prescription including photosensitive)

Public Device Record Key

7f22d938-4686-4e07-b0b6-4d0f3255ebe3

Public Version Date

February 07, 2022

Public Version Number

1

DI Record Publish Date

January 30, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-