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Kangaroo

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
Kangaroo Purple Enteral Feeding Syringe Tip Cap FDA UDI
Model / Reference
401S FDA UDI
Description
Kangaroo Purple Enteral Feeding Syringe Tip Cap FDA UDI

Identifiers

Catalog Number
401S FDA UDI
Primary DI / UDI-DI
20192253007425 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENFit oral/enteral syringe, single-use

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

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 34b6f851-58de-4cd6-8631-5bb17750342c 34 fields · synced Jun 8, 2026