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

HIL

Product Code Name

TAMPON, MENSTRUAL, SCENTED, DEODORIZED

Public Device Record Key

772007a5-1493-44f0-bb58-2426123d5e16

Public Version Date

August 15, 2022

Public Version Number

5

DI Record Publish Date

February 27, 2017

Package DI Number

10073010711348

Quantity per Package

6

Contains DI Package

00073010711341

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case