Catalog Number

773621

Brand Name

Kangaroo

Version/Model Number

773621

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"

-

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

FRN

Product Code Name

Pump, infusion

Public Device Record Key

6ad6af11-03c1-4314-a58f-5922e7ec3cb0

Public Version Date

October 28, 2019

Public Version Number

7

DI Record Publish Date

September 24, 2016

Package DI Number

20884521000831

Quantity per Package

30

Contains DI Package

10884521000834

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE