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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Medical device adhesive FDA UDI
Device Name
CO2 Detector with Bellows FDA UDI
Model / Reference
777702 FDA UDI
Description
CO2 Detector with Bellows FDA UDI

Identifiers

Catalog Number
777702 FDA UDI
Primary DI / UDI-DI
30884521000272 FDA UDI
510(k) Number
K042572 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Medical device adhesive 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

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: Medical device adhesive

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

Similar devices

Also classified as Medical device adhesive.

Cleared under the same submission

K042572 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI b24e86a0-b41c-4b6b-bdcc-5f77ae3ddc8e 37 fields · synced May 30, 2026