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I13C3f Transducer 9076

by Bk Medical ApS

Ref 9076

I13C3f Transducer 9076 is a device classified as Class IIa in the EU and Class II in the US made by Bk Medical ApS, registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI B-05704916000240) and listed in FDA GUDID since 26 Mar 2020 (UDI-DI 05704916000240), 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-05704916000240 Basic UDI-DI 05704916000240UDI-DIDate16 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05704916000240 UDI-DI Date26 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05704916000240 registered 16 Jul 2026 Active
  • FDA GUDID UDI-DI 05704916000240 listed 26 Mar 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05704916000240
  2. Registered EUDAMED B-05704916000240

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  • Withdrawn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
I13C3f EUDAMED
I13C3f Transducer GUDID
Generic name
Surgical ultrasound imaging transducer
Model / reference
9076
Primary DI / UDI-DI
05704916000240
Basic UDI-DI
B-05704916000240
FDA product code
ITX
EMDN code
Z11040299 Ultrasound probes – other
GMDN term
Surgical ultrasound imaging transducer
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
892.1570
EU registration type
Legacy device (under a directive)
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Surgical ultrasound imaging transducer

Similar devices in this category

Other devices filed under ULTRASOUND PROBES – OTHER.

Other devices from Bk Medical ApS

See all devices from Bk Medical ApS →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (19, all answered No)