Catalog Number

100025

Brand Name

EPAD

Version/Model Number

EPAD

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 10, 2019

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GWF

Product Code Name

Stimulator, Electrical, Evoked Response

Public Device Record Key

f1937147-052e-419e-8145-85e3b8384faa

Public Version Date

August 30, 2021

Public Version Number

3

DI Record Publish Date

May 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-