Catalog Number

-

Brand Name

Preference

Version/Model Number

11002

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HEB

Product Code Name

Tampon, Menstrual, Unscented

Public Device Record Key

bad01249-ba20-4003-a760-3b9ec188da86

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

October 30, 2019

Package DI Number

10710865000035

Quantity per Package

12

Contains DI Package

00710865000038

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case