Skip to content

Maico MA 1

by MAICO Diagnostics GmbH

Ref 8000183

Maico MA 1 is a device classified as Class IIa in the EU and Class II in the US made by MAICO Diagnostics GmbH, registered in EUDAMED on 20 Aug 2026 (Basic UDI-DI 426017612_8000183_WW) and listed in FDA GUDID since 17 Apr 2020 (UDI-DI 04260176120858), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number426017612_8000183_WW Basic UDI-DI 04260176120858UDI-DIDate20 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04260176120858 UDI-DI Date17 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 426017612_8000183_WW registered 20 Aug 2026 Active
  • FDA GUDID UDI-DI 04260176120858 listed 17 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04260176120858
  2. Registered EUDAMED 426017612_8000183_WW

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  • Withdrawn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
Ma 1 EUDAMED
Maico GUDID
Generic name
Tone audiometer
Model / reference
8000183 EUDAMED
MA 1 GUDID
Primary DI / UDI-DI
04260176120858
Basic UDI-DI
426017612_8000183_WW
Direct marketing DI
04260176120858
FDA product code
EWO
EMDN code
Z121401 Audiometers
GMDN term
Tone audiometer
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
874.1050
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
8000183
GUDID
MA 1
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: Tone audiometer

Similar devices in this category

Other devices filed under AUDIOMETERS.

Other devices from Maico Diagnostic GmbH

See all devices from Maico Diagnostic GmbH →

Properties

  • Measuring function
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)