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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
Personal device holder, reusable FDA UDI
Device Name
KANGAROO JOEY BLUE MINI BACKPACK FDA UDI
Model / Reference
770026 FDA UDI
Description
KANGAROO JOEY BLUE MINI BACKPACK FDA UDI

Identifiers

Catalog Number
770026 FDA UDI
Primary DI / UDI-DI
10192253009712 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Personal device holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Personal device holder, reusable

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

Similar devices

Also classified as Personal device holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 716134c4-317b-4cd3-b5ef-1e115c17b34e 34 fields · synced Jun 8, 2026