AccessGUDID - DEVICE: Kangaroo (10192253011302)

GUDID

Device Identifier (DI) Information

Brand Name: Kangaroo
Version or Model: 8884711501
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 8884711501
Company Name: Cardinal Health 200, LLC

Primary DI Number: 10192253011302
Issuing Agency: GS1
Commercial Distribution End Date: March 31, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 961027315 *Terms of Use

Device Description: Feeding Tube

Device Characteristics

What MRI safety information does the labeling contain?	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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
16798	Nasoenteral tube	A sterile, thin, flexible, hollow cylinder designed to access the small intestines (duodenum or jejunum) through the nose and nasopharynx for examination (e.g., of intestinal contents), treatment (e.g., decompression, short-term feeding), or other purposes. It is a single- or dual-lumen, rubber or plastic tube (nasoduodenal or nasojejunal tube) that is smaller and longer than a nasogastric tube and may have a small weight or magnet at the distal tip to facilitate placement. It is frequently used for very ill or comatose patients. Some types are used to remove air and liquids from the stomach by connection to intermittent suction units and/or for enteral feeding. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNT	Tubes, gastrointestinal (and accessories)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Length: 91 Centimeter
Catheter Gauge: 12 French

Device Record Status

Public Device Record Key: 5da7fba0-1ffe-47c1-8f3c-ae17ca7227b1
Public Version Date: July 29, 2025
Public Version Number: 3
DI Record Publish Date: January 23, 2024