Kangaroo - Insufflation Device. For use with ENFit - Cardinal Health, Inc.

Duns Number:080935429

Device Description: Insufflation Device. For use with ENFit Connection System. For use with Kangaroo Feeding T Insufflation Device. For use with ENFit Connection System. For use with Kangaroo Feeding Tubes with IRIS Technology

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More Product Details

Catalog Number

388105E

Brand Name

Kangaroo

Version/Model Number

388105E

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)

-

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

KNT

Product Code Name

TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Device Record Status

Public Device Record Key

3ac358f1-d4e1-4ae5-a708-eb82c9a73a47

Public Version Date

June 17, 2019

Public Version Number

8

DI Record Publish Date

April 20, 2017

Additional Identifiers

Package DI Number

10884521706170

Quantity per Package

5

Contains DI Package

20884521706177

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"CARDINAL HEALTH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 672
2 A medical device with a moderate to high risk that requires special controls. 1692
U Unclassified 17