Catalog Number

45100

Brand Name

Seventh Generation

Version/Model Number

Regular, no applicator

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

HEB

Product Code Name

Tampon, Menstrual, Unscented

Public Device Record Key

fdc6c0de-b7e4-421b-b297-60cc7c0d2aeb

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

September 08, 2016

Package DI Number

10732913451002

Quantity per Package

12

Contains DI Package

00732913451005

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case