Catalog Number

-

Brand Name

DR. MERCOLA

Version/Model Number

Ultra Day Pads

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

HHD

Product Code Name

Pad, Menstrual, Unscented

Public Device Record Key

792fe1b8-1f53-40ef-8c76-d953bd411b2e

Public Version Date

January 05, 2021

Public Version Number

1

DI Record Publish Date

December 28, 2020

Package DI Number

10813006012710

Quantity per Package

12

Contains DI Package

00813006012713

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Cardboard