Catalog Number

ET-8080

Brand Name

iReliev

Version/Model Number

ET-8080

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NGX

Product Code Name

Stimulator, Muscle, Powered, For Muscle Conditioning

Public Device Record Key

d59910ab-fffa-4bc6-be3c-a7e15441cb38

Public Version Date

February 19, 2021

Public Version Number

4

DI Record Publish Date

July 20, 2018

Package DI Number

20853635002741

Quantity per Package

40

Contains DI Package

00853635002747

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton