Catalog Number

-

Brand Name

Technomed Europe

Version/Model Number

TE/K50430-001

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

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

9432ac9e-d4a5-4f6b-a476-ecf0918c6597

Public Version Date

July 03, 2020

Public Version Number

1

DI Record Publish Date

June 25, 2020

Package DI Number

08718375861134

Quantity per Package

10

Contains DI Package

08718375862940

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelf box