Catalog Number

-

Brand Name

Maxithins

Version/Model Number

BCNABSMXO20

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

c401a717-89b8-49c4-aaef-b3d42ff2b213

Public Version Date

May 23, 2022

Public Version Number

2

DI Record Publish Date

May 01, 2020

Package DI Number

10187933656201

Quantity per Package

6

Contains DI Package

00187933656204

Package Discontinue Date

May 01, 2022

Package Status

Not in Commercial Distribution

Package Type

Case