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533624

by inomed Medizintechnik GmbH

Ref 533624

533624 is a device classified as Class IIa in the EU and Class II in the US made by inomed Medizintechnik GmbH, registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI B-04250307604135) and listed in FDA GUDID since 20 Oct 2023 (UDI-DI 04250307604135), 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-04250307604135 Basic UDI-DI 04250307604135UDI-DIDate21 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250307604135 UDI-DI Date20 Oct 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250307604135 registered 21 Sep 2026 Active
  • FDA GUDID UDI-DI 04250307604135 listed 20 Oct 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250307604135
  2. Registered EUDAMED B-04250307604135

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  • Withdrawn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
SDN Elektrode GR 15/1000, Edelstahl
Generic name
Electromyographic needle electrode, single-use
Model / reference
533624
Primary DI / UDI-DI
04250307604135
Basic UDI-DI
B-04250307604135
FDA product code
GWF
EMDN code
N010180 Neurophysiology devices - accessories
GMDN term
Electromyographic needle electrode, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
882.1870
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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: Electromyographic needle electrode, single-use

Similar devices in this category

Other devices filed under NEUROPHYSIOLOGY DEVICES - ACCESSORIES.

Other devices from inomed Medizintechnik GmbH

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)