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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Basic power supply, reusable FDA UDI
Device Name
Replacement Battery For use with Kangaroo Feeding Tubes with IRIS Technology FDA UDI
Model / Reference
388102 FDA UDI
Description
Replacement Battery For use with Kangaroo Feeding Tubes with IRIS Technology FDA UDI

Identifiers

Catalog Number
388102 FDA UDI
Primary DI / UDI-DI
10884521165007 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Basic power supply, reusable

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

Similar devices

Also classified as Basic power supply, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI f2268721-5821-4766-8fbf-3e132f99dbaa 37 fields · synced May 30, 2026