Catalog Number

-

Brand Name

Best Choice

Version/Model Number

BUSBCSDMXR24

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

NRC

Product Code Name

Pads, Menstrual, Scented-Deodorized

Public Device Record Key

d0da6fa4-ae11-4b40-ba92-ed22705aeb2e

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

June 01, 2020

Package DI Number

10070038202971

Quantity per Package

12

Contains DI Package

00070038202974

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE