Catalog Number

-

Brand Name

MobileECG System

Version/Model Number

MobileECG System

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

November 15, 2029

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

-

Product Code Name

-

Public Device Record Key

5fc353ee-9202-4626-b1ec-b6b5844402af

Public Version Date

March 10, 2021

Public Version Number

2

DI Record Publish Date

November 15, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-