Catalog Number

-

Brand Name

Equate

Version/Model Number

STT

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

JEQ

Product Code Name

Toothbrush, Powered

Public Device Record Key

aa7da02b-99dc-4df4-aea6-4dc1e7f2e0be

Public Version Date

July 07, 2020

Public Version Number

2

DI Record Publish Date

June 17, 2020

Package DI Number

40078742122678

Quantity per Package

6

Contains DI Package

00078742122670

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

inner