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USB Cable 0.4m USB-CAB-2

by Otodynamics

Part of a family of 7 devices: see the family page

Ref USB-CAB-04Model USBCAB

USB Cable 0.4m USB-CAB-2 is a device classified as Class I in the EU and Class II in the US made by Otodynamics, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 506039617USBCABDY) and listed in FDA GUDID since 15 Jul 2016 (UDI-DI 05060396170690), active as of 7 Nov 2026.

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

CE MDR

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number506039617USBCABDY Basic UDI-DI 05060396170690UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060396170690 UDI-DI Date15 Jul 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 506039617USBCABDY registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 05060396170690 listed 15 Jul 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060396170690
  2. Registered EUDAMED 506039617USBCABDY

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
USB Cable 0.4m
Generic name
Otoacoustic emission system, line-powered
Device name
Otodynamics USB Cables
Model / reference
USBCAB EUDAMED
USB-CAB-04 EUDAMED
USB-CAB-2 GUDID
Primary DI / UDI-DI
05060396170690
Basic UDI-DI
506039617USBCABDY
Direct marketing DI
05060396170690
FDA product code
EWO
EMDN code
Z12149001 Otoacoustic emissions equipment
GMDN term
Otoacoustic emission system, line-powered
Device class
Class I EUDAMED
Class II GUDID
Regulation number
874.1050
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
USBCAB
USB-CAB-04
GUDID
USB-CAB-2
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Otoacoustic emission system, line-powered

Similar devices in this category

Other devices filed under OTOACOUSTIC EMISSIONS EQUIPMENT.

Other devices from Otodynamics

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Properties

  • Premarket exempt
Other properties (24, all answered No)