Catalog Number

-

Brand Name

Veeda

Version/Model Number

VDTS32US

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

K130609,K130609,K130609,K130609

Product Code

HEB

Product Code Name

Tampon, Menstrual, Unscented

Public Device Record Key

f2c4b3eb-2af0-4747-bcec-79af20b2b2a4

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

April 30, 2018

Package DI Number

10810462021546

Quantity per Package

8

Contains DI Package

20810462021543

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case