Catalog Number

384500CBW

Brand Name

Kangaroo

Version/Model Number

384500CBW

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

LZH

Product Code Name

PUMP, INFUSION, ENTERAL

Public Device Record Key

1db7302d-a7a7-464c-8b92-59ae186ca6fa

Public Version Date

February 15, 2019

Public Version Number

5

DI Record Publish Date

July 04, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-