← Back to catalogue

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 Feeding Set with Flush Bag 500mL FDA UDI
Model / Reference
B5FF FDA UDI
Description
Kangaroo Omni Feeding Set with Flush Bag 500mL FDA UDI

Identifiers

Catalog Number
B5FF FDA UDI
Primary DI / UDI-DI
10885380177132 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 58be952c-81ec-49a8-9eb2-3c5b61029a5a 35 fields · synced Jun 6, 2026