Catalog Number

-

Brand Name

MediMax Tech

Version/Model Number

CF90RT Tens Electrode

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

45d2173a-583c-49f8-9a59-e58e78a8a09e

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

August 03, 2016

Package DI Number

30817325020580

Quantity per Package

5

Contains DI Package

20817325020583

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case