CARDINAL HEALTH - CABG,KIT - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: CABG,KIT

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More Product Details

Catalog Number

PC12CGMWC

Brand Name

CARDINAL HEALTH

Version/Model Number

PC12CGMWC

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

OEZ

Product Code Name

Cardiovascular procedure kit

Device Record Status

Public Device Record Key

29d14cde-729f-4611-8fc6-0290256452b2

Public Version Date

July 23, 2018

Public Version Number

3

DI Record Publish Date

August 31, 2015

Additional Identifiers

Package DI Number

50885425960444

Quantity per Package

1

Contains DI Package

00885425960449

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"CARDINAL HEALTH 200, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 101686
2 A medical device with a moderate to high risk that requires special controls. 139430
3 A medical device with high risk that requires premarket approval 8
U Unclassified 40