Catalog Number

-

Brand Name

Tampax

Version/Model Number

Cup

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

-

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

HHE

Product Code Name

Cup, menstrual

Public Device Record Key

e50845ed-e440-4a05-864e-723e9d00ae9e

Public Version Date

July 07, 2020

Public Version Number

2

DI Record Publish Date

October 01, 2018

Package DI Number

40073010713268

Quantity per Package

150

Contains DI Package

00073010713260

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pallet