Catalog Number

23-0051

Brand Name

Spacelabs Healthcare

Version/Model Number

EVENTREC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

DXH

Product Code Name

TRANSMITTERS AND RECEIVERS, ELECTROCARDIOGRAPH, TELEPHONE

Public Device Record Key

b39027ea-2cd0-4de7-a197-b51587725fc7

Public Version Date

March 04, 2019

Public Version Number

1

DI Record Publish Date

February 01, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-