Catalog Number

-

Brand Name

ViaMed

Version/Model Number

13210

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K041954,K041954

Product Code

DRX

Product Code Name

Electrode, Electrocardiograph

Public Device Record Key

9706d256-f3ca-470b-8e1f-0773657ca413

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 18, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-