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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Enteral feeding noninvasive-component set FDA UDI
Device Name
Connect Feeding Set,Anti-free Flow FDA UDI
Model / Reference
77500FD FDA UDI
Description
Connect Feeding Set,Anti-free Flow FDA UDI

Identifiers

Catalog Number
77500FD FDA UDI
Primary DI / UDI-DI
10884521190849 FDA UDI
FDA Product Code
LZH FDA UDI
GMDN Term
Enteral feeding noninvasive-component set 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter FDA UDI

Category: Enteral feeding noninvasive-component set

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

Similar devices

Also classified as Enteral feeding noninvasive-component set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI cf1d6e7c-b46e-45dd-9273-8d8dad5e91f4 37 fields · synced May 30, 2026