Catalog Number

8884721252E

Brand Name

Kangaroo

Version/Model Number

8884721252E

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

d465a0bb-9503-49ec-8435-3cb6dd61166d

Public Version Date

November 02, 2020

Public Version Number

7

DI Record Publish Date

July 04, 2017

Package DI Number

20884521583037

Quantity per Package

10

Contains DI Package

10884521583030

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE