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devemed 2583

by devemed GmbH

Part of a family of 6 devices: see the family page

Ref 2583

devemed 2583 is a Class I device made by devemed GmbH, registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 4061644PG1102CE) and listed in FDA GUDID since 1 May 2020 (UDI-DI 04061644005284), 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 Number4061644PG1102CE Basic UDI-DI 04061644005284UDI-DIDate14 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04061644005284 UDI-DI Date1 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4061644PG1102CE registered 14 Jul 2026 Active
  • FDA GUDID UDI-DI 04061644005284 listed 1 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04061644005284
  2. Registered EUDAMED 4061644PG1102CE

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  • Withdrawn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
devemed
Generic name
Dental articulation paper forceps
Device name
Tweezers for articulating paper
Model / reference
2583
Primary DI / UDI-DI
04061644005284
Basic UDI-DI
4061644PG1102CE
Direct marketing DI
04061644005284
FDA product code
EFK
EMDN code
L150399 Odontostomatology forceps, reusable - other
GMDN term
Dental articulation paper forceps
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental articulation paper forceps

Similar devices in this category

Other devices filed under ODONTOSTOMATOLOGY FORCEPS, REUSABLE - OTHER.

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)