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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Nasoenteral tube FDA UDI
Device Name
Feeding Tube,Dual Port with Radiopaque Line, Non-weighted FDA UDI
Model / Reference
8884711568 FDA UDI
Description
Feeding Tube,Dual Port with Radiopaque Line, Non-weighted FDA UDI

Identifiers

Catalog Number
8884711568 FDA UDI
Primary DI / UDI-DI
10884521009714 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasoenteral tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 8 French FDA UDI
Length — 36 Inch FDA UDI

Category: Nasoenteral tube

Kangaroo by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasoenteral tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI e18f03a1-c802-4071-9d99-42316bdf7434 37 fields · synced Jun 8, 2026