Catalog Number

-

Brand Name

Maxithins

Version/Model Number

BUSABSDMXS24

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 01, 2022

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

NRC

Product Code Name

Pads, Menstrual, Scented-Deodorized

Public Device Record Key

71777ee1-f874-40d8-9835-ba92ded92081

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

May 01, 2020

Package DI Number

10075289580540

Quantity per Package

12

Contains DI Package

00075289580543

Package Discontinue Date

May 01, 2022

Package Status

Not in Commercial Distribution

Package Type

Case