Catalog Number

-

Brand Name

Flents

Version/Model Number

68081

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

aebcd770-3d96-4d74-82b2-824ac9e3f5bd

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

November 24, 2020

Package DI Number

20025715036346

Quantity per Package

4

Contains DI Package

00025715680811

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

INNER