Catalog Number

-

Brand Name

Freshmint

Version/Model Number

DF12

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

-

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

JES

Product Code Name

Floss, Dental

Public Device Record Key

80b5d699-c78c-41e4-8210-4d3e4f175164

Public Version Date

August 19, 2020

Public Version Number

1

DI Record Publish Date

August 11, 2020

Package DI Number

00085317003739

Quantity per Package

12

Contains DI Package

00085317007942

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Bag