Catalog Number

-

Brand Name

Tampax

Version/Model Number

Tampax Pearl

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

c203749e-abd1-42c3-b244-7f9917c4c3d3

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

June 27, 2018

Package DI Number

40073010023787

Quantity per Package

8

Contains DI Package

00073010023789

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pallet