Catalog Number

762000

Brand Name

Kangaroo

Version/Model Number

762000

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

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

KNT

Product Code Name

TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Public Device Record Key

9327681f-6562-4141-baa1-4e8ec662bcc3

Public Version Date

April 20, 2020

Public Version Number

9

DI Record Publish Date

September 24, 2016

Package DI Number

30884521020164

Quantity per Package

2

Contains DI Package

40884521020161

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE