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Gyrus ACMI 24BX

by Gyrus Acmi, Inc.

Ref 24BX

Gyrus ACMI 24BX is a device classified as Class IIa in the EU and Class I in the US made by Gyrus Acmi, Inc., registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI B-00821925010109) and listed in FDA GUDID since 11 Sep 2018 (UDI-DI 00821925010109), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00821925010109 Basic UDI-DI 00821925010109UDI-DIDate8 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00821925010109 UDI-DI Date11 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00821925010109 registered 8 Oct 2026 Active
  • FDA GUDID UDI-DI 00821925010109 listed 11 Sep 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00821925010109
  2. Registered EUDAMED B-00821925010109

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  • Withdrawn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
Gyrus ACMI
Generic name
Gastro-urological guidewire, single-use
Device name
24BX
Model / reference
24BX
Primary DI / UDI-DI
00821925010109 EUDAMED
00821925003842 GUDID
Basic UDI-DI
B-00821925010109
FDA product code
EYA
EMDN code
U0602 Urological guidewires, not hydrophilic
GMDN term
Gastro-urological guidewire, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
876.5130
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00821925010109
GUDID
00821925003842
Device classEUDAMED
Class IIa
GUDID
Class I

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00821925010109; FDA GUDID lists 00821925003842), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Gastro-urological guidewire, single-use

Similar devices in this category

Other devices filed under UROLOGICAL GUIDEWIRES.

Other devices from Gyrus Acmi, Inc.

See all devices from Gyrus Acmi, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)