Catalog Number

9607-0218

Brand Name

Zephyr

Version/Model Number

9607-0218

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 26, 2018

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

DRX

Product Code Name

Electrode, electrocardiograph

Public Device Record Key

8dbcb4cf-edb2-46ec-b881-f0bd386faff9

Public Version Date

March 10, 2021

Public Version Number

5

DI Record Publish Date

January 24, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-