Catalog Number

-

Brand Name

Leader

Version/Model Number

11244

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

EWD

Product Code Name

Protector, Hearing (Insert)

Public Device Record Key

ebd3bb2f-032d-4336-b2fc-fea9b26b1b63

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

March 21, 2019

Package DI Number

10096295133872

Quantity per Package

1

Contains DI Package

00096295133875

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

unit