Catalog Number

-

Brand Name

Exchange Select Tampons

Version/Model Number

BAFGS18

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

2a606b27-ae69-42ab-a0c8-8702a27eb6eb

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

September 20, 2016

Package DI Number

10614299402062

Quantity per Package

12

Contains DI Package

00614299402065

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE