Catalog Number

SAN23PEMUQ

Brand Name

CARDINAL HEALTH

Version/Model Number

SAN23PEMUQ

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"

Yes

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

OES

Product Code Name

Cardiac catheterization kit

Public Device Record Key

7f1ee795-3fa4-42fd-a513-afad8c497735

Public Version Date

July 20, 2018

Public Version Number

3

DI Record Publish Date

August 07, 2015

Package DI Number

50885425852602

Quantity per Package

2

Contains DI Package

00885425852607

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE