Catalog Number

-

Brand Name

MYI OCCLUSION EYE PATCHES

Version/Model Number

007

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HOY

Product Code Name

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

Public Device Record Key

cc4b2230-9ee5-4096-96bc-c0e5deef63cc

Public Version Date

June 28, 2021

Public Version Number

5

DI Record Publish Date

March 29, 2021

Package DI Number

10850029104558

Quantity per Package

3

Contains DI Package

00850029104018

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PACKETS of 17