Catalog Number

-

Brand Name

Veeda

Version/Model Number

VPLFO40US

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

HHD

Product Code Name

Pad, Menstrual, Unscented

Public Device Record Key

af784a6a-cd00-4ff1-b257-08c8f05ed533

Public Version Date

May 23, 2019

Public Version Number

2

DI Record Publish Date

September 26, 2018

Package DI Number

00810462021402

Quantity per Package

4

Contains DI Package

00810462020450

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case