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Kangaroo 720250

by Cardinalhealth

Ref 720250

Kangaroo 720250 is a gastrostomy tube (EU MDD Class IIb; FDA Class II; FDA product code KNT, Tubes, Gastrointestinal (and Accessories)) made by Cardinalhealth, registered in EUDAMED on 21 May 2026 (Basic UDI-DI B-10884521011298) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521011298), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10884521011298 Basic UDI-DI 10884521011298UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521011298 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10884521011298 registered 21 May 2026 Active
  • FDA GUDID UDI-DI 10884521011298 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521011298
  2. Registered EUDAMED B-10884521011298

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Kangaroo
Generic name
Gastrostomy tube
Model / Ref / Catalog
720250
Primary DI / UDI-DI
10884521011298
Basic UDI-DI
B-10884521011298
FDA product code
KNT
EMDN code
G02020201 Gastrostomy, tubes and sets
GMDN term
Gastrostomy tube
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
876.5980
EU registration type
Legacy device (under a directive)
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 20 French
Length — 2.5 Centimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
ImplantableEUDAMED
No
GUDID
Yes

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Gastrostomy tube

Similar devices in this category

Other devices filed under GASTROSTOMY, TUBES AND SETS.

Other devices from Cardinalhealth

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Properties

  • Supplied sterile
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Administering medicine
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)