← Back to catalogue

Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Exhaled-gas oesophageal intubation detector FDA UDI
Device Name
CO2 Detector with Bellows FDA UDI
Model / Reference
777702E FDA UDI
Description
CO2 Detector with Bellows FDA UDI

Identifiers

Catalog Number
777702E FDA UDI
Primary DI / UDI-DI
10884521724129 FDA UDI
510(k) Number
K042572 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Exhaled-gas oesophageal intubation detector 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: Exhaled-gas oesophageal intubation detector

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

Similar devices

Also classified as Exhaled-gas oesophageal intubation detector.

Cleared under the same submission

K042572 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 81206f26-e910-4298-9598-3197ae54eeb0 37 fields · synced Jun 6, 2026