Catalog Number

-

Brand Name

365

Version/Model Number

WH32006F/1

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

bb9f2f72-d735-4d7d-b31a-441433b3ec0a

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

July 05, 2017

Package DI Number

10099482438019

Quantity per Package

6

Contains DI Package

00099482438012

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE