Catalog Number

520007P

Brand Name

N/A

Version/Model Number

520007P

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LDF

Product Code Name

ELECTRODE, PACEMAKER, TEMPORARY

Public Device Record Key

de7f00cd-0c6d-4459-8dd1-955403c14111

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 29, 2015

Package DI Number

10801741011532

Quantity per Package

5

Contains DI Package

00801741011535

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA