Catalog Number

ESLF5050

Brand Name

EASLIEF

Version/Model Number

ESLF5050

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)

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

6dd12679-daeb-47af-b265-438be81e1666

Public Version Date

February 19, 2021

Public Version Number

4

DI Record Publish Date

January 12, 2018

Package DI Number

10851610008255

Quantity per Package

80

Contains DI Package

00851610008258

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box