Catalog Number

8884720825E

Brand Name

Kangaroo

Version/Model Number

8884720825E

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

fdc10028-0cec-47ef-80f8-360ab45efbf1

Public Version Date

November 02, 2020

Public Version Number

7

DI Record Publish Date

July 04, 2017

Package DI Number

20884521582948

Quantity per Package

10

Contains DI Package

10884521582941

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE