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devemed 2693

by devemed GmbH

Part of a family of 35 devices: see the family page

Ref 2693

devemed 2693 is a Class I device made by devemed GmbH, registered in EUDAMED on 13 Jul 2026 (Basic UDI-DI 4061644PG1105032P) and listed in FDA GUDID since 1 May 2020 (UDI-DI 04061644005550), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4061644PG1105032P Basic UDI-DI 04061644005550UDI-DIDate13 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04061644005550 UDI-DI Date1 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4061644PG1105032P registered 13 Jul 2026 Active
  • FDA GUDID UDI-DI 04061644005550 listed 1 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04061644005550
  2. Registered EUDAMED 4061644PG1105032P

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  • Withdrawn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 prosthesis removal instrument
Device name
Crown Pliers
Model / reference
2693
Description
Silicone insert for Art No 2709 (1 pc)
Primary DI / UDI-DI
04061644005550
Basic UDI-DI
4061644PG1105032P
Direct marketing DI
04061644005550
FDA product code
EIS
EMDN code
Q010299 Prosthetic dentistry devices - other
GMDN term
Dental prosthesis removal instrument
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

Similar devices in this category

Other devices filed under PROSTHETIC DENTISTRY DEVICES - 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)