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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
Bedside syringe pump FDA UDI
Device Name
Kangaroo LTE Wireless Communication Hub FDA UDI
Model / Reference
384505CBC FDA UDI
Description
Kangaroo LTE Wireless Communication Hub FDA UDI

Identifiers

Catalog Number
384505CBC FDA UDI
Primary DI / UDI-DI
10885380184383 FDA UDI
FDA Product Code
LZH FDA UDI
GMDN Term
Bedside syringe 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

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bedside syringe pump

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

Similar devices

Also classified as Bedside syringe 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 afa88f48-2e85-4c4f-83ef-bf32501c7c82 34 fields · synced Jun 8, 2026