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Enteral NCF05.60

by GBUK Group, Ltd.

Ref NCF05.60

Enteral NCF05.60 is a device classified as Class IIb in the EU and Class II in the US made by GBUK Group, Ltd., registered in EUDAMED on 14 Aug 2026 (Basic UDI-DI B-05060590884577) and listed in FDA GUDID since 1 Nov 2022 (UDI-DI 05060590884577), 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-05060590884577 Basic UDI-DI 05060590884577UDI-DIDate14 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060590884577 UDI-DI Date1 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05060590884577 registered 14 Aug 2026 Active
  • FDA GUDID UDI-DI 05060590884577 listed 1 Nov 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060590884577
  2. Registered EUDAMED B-05060590884577

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  • Withdrawn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
Enteral
Generic name
Nasogastric feeding tube
Model / Ref / Catalog
NCF05.60
Primary DI / UDI-DI
05060590884577
Basic UDI-DI
B-05060590884577
FDA product code
PIF
EMDN code
G02020101 Nasogastric tubes
GMDN term
Nasogastric feeding 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
Germany
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

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: Nasogastric feeding tube

Similar devices in this category

Other devices filed under NASOGASTRIC TUBES.

Other devices from GBUK Group, Ltd.

See all devices from GBUK Group, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Administering medicine
  • Measuring function
  • Lot / batch number
  • Serial number
Other properties (19, all answered No)