Catalog Number

221-28SS-730

Brand Name

Chalgren

Version/Model Number

221-28SS-730

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

Yes

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

IKT

Product Code Name

Electrode, Needle, Diagnostic Electromyograph

Public Device Record Key

f12a7c76-3985-4c38-a60d-972c7ce8a0a0

Public Version Date

June 11, 2018

Public Version Number

3

DI Record Publish Date

September 10, 2016

Package DI Number

40816020020366

Quantity per Package

20

Contains DI Package

00816020020368

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box