Catalog Number

-

Brand Name

Carefree

Version/Model Number

03100

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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)

-

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

1f47937a-e70d-4862-ab3a-ffa3dee07f83

Public Version Date

May 23, 2019

Public Version Number

2

DI Record Publish Date

April 30, 2019

Package DI Number

10078300031007

Quantity per Package

6

Contains DI Package

00078300031000

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-