Catalog Number

-

Brand Name

Moxie

Version/Model Number

MUS007

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

f53d32e1-f65e-4774-b9ab-30ede77ea2dd

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

October 24, 2016

Package DI Number

59336798000899

Quantity per Package

12

Contains DI Package

09336798000894

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-