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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Sump drain FDA UDI
Device Name
Multi-functional Port with Single Lumen Adapter FDA UDI
Model / Reference
771111 FDA UDI
Description
Multi-functional Port with Single Lumen Adapter FDA UDI

Identifiers

Catalog Number
771111 FDA UDI
Primary DI / UDI-DI
10884521004184 FDA UDI
FDA Product Code
FEG FDA UDI
GMDN Term
Sump drain 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

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

No

FDA UDI

Category: Sump drain

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

Similar devices

Also classified as Sump drain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI def324e4-a196-411b-a405-e78c06bcd975 36 fields · synced May 30, 2026