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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
ENFit/non-ISO80369-standardized linear connector FDA UDI
Device Name
Kangaroo ENFit Transition Connector FDA UDI
Model / Reference
765000 FDA UDI
Description
Kangaroo ENFit Transition Connector FDA UDI

Identifiers

Catalog Number
765000- FDA UDI
Primary DI / UDI-DI
10192253009644 FDA UDI
FDA Product Code
PIO FDA UDI
GMDN Term
ENFit/non-ISO80369-standardized linear connector 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: ENFit/non-ISO80369-standardized linear connector

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

Similar devices

Also classified as ENFit/non-ISO80369-standardized linear connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI f15d6c76-4fc1-4579-bd22-020d6d4dd82b 34 fields · synced Jun 8, 2026