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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
Anaesthesia face mask, reusable FDA UDI
Device Name
FEEDING TUBE IRRIG KIT ENFIT FDA UDI
Model / Reference
8884700108E FDA UDI
Description
FEEDING TUBE IRRIG KIT ENFIT FDA UDI

Identifiers

Catalog Number
8884700108E FDA UDI
Primary DI / UDI-DI
10192253011036 FDA UDI
FDA Product Code
PNR FDA UDI
GMDN Term
Anaesthesia face mask, reusable 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Dimensions & Sizes

Size
Total Volume — 60 Milliliter FDA UDI

Category: Anaesthesia face mask, reusable

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

Similar devices

Also classified as Anaesthesia face mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 310724da-fb4d-47cb-8ba6-4419c741599b 35 fields · synced Jun 8, 2026