Catalog Number

-

Brand Name

DG Health

Version/Model Number

BDGGS36

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

c4c7d087-a2e0-4979-9154-732c6da6b3d3

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 18, 2021

Package DI Number

10834533001015

Quantity per Package

4

Contains DI Package

00834533001018

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE