Catalog Number

-

Brand Name

Equate

Version/Model Number

ZQG

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

23d53e7b-d84e-4a9b-9ee2-e27404cb89d2

Public Version Date

July 07, 2020

Public Version Number

2

DI Record Publish Date

June 23, 2020

Package DI Number

20681131129095

Quantity per Package

36

Contains DI Package

00681131129091

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case