Catalog Number

-

Brand Name

MEIJER

Version/Model Number

419310

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

e09e53f6-110a-4eb7-86fb-18b23454fe31

Public Version Date

September 10, 2020

Public Version Number

1

DI Record Publish Date

September 02, 2020

Package DI Number

10708820656366

Quantity per Package

6

Contains DI Package

00708820656369

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipping Case