Catalog Number

-

Brand Name

Flents

Version/Model Number

69018

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

29e4f15d-73c1-4b07-92f9-141016303636

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

November 12, 2021

Package DI Number

10025715029860

Quantity per Package

24

Contains DI Package

00025715690186

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case