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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Enteral feeding pump FDA UDI
Device Name
Connect Wi-Fi/Ethernet Communications Module Power Adapter FDA UDI
Model / Reference
384500CBW FDA UDI
Description
Connect Wi-Fi/Ethernet Communications Module Power Adapter FDA UDI

Identifiers

Catalog Number
384500CBW FDA UDI
Primary DI / UDI-DI
10884521190962 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 Cardinalhealth — 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
Cardinalhealth

Sources (1)

  • FDA UDI 1db7302d-a7a7-464c-8b92-59ae186ca6fa 36 fields · synced May 30, 2026