Catalog Number

-

Brand Name

Maxithins

Version/Model Number

FCNABSPLL32

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

HHD

Product Code Name

Pad, Menstrual, Unscented

Public Device Record Key

4bab2d90-bdb5-4149-86db-b71d5534b893

Public Version Date

May 23, 2022

Public Version Number

2

DI Record Publish Date

June 01, 2020

Package DI Number

10075289110327

Quantity per Package

48

Contains DI Package

00075289110320

Package Discontinue Date

May 01, 2022

Package Status

Not in Commercial Distribution

Package Type

CASE