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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Enteral feeding pump FDA UDI
Device Name
Kangaroo Omni Enteral Feeding Pump with RF chip - Refurbished FDA UDI
Model / Reference
385401 FDA UDI
Description
Kangaroo Omni Enteral Feeding Pump with RF chip - Refurbished FDA UDI

Identifiers

Catalog Number
385401 FDA UDI
Primary DI / UDI-DI
10885380184567 FDA UDI
FDA Product Code
LZH FDA UDI
GMDN Term
Enteral feeding pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Enteral feeding pump

Kangaroo by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral feeding pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 026b5e51-f801-49c0-9027-e90978505970 35 fields · synced Jun 8, 2026