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LEDview plus 6481464

by SIRONA Dental Systems GmbH

Ref 6481464

LEDview plus 6481464 is a Class I device made by SIRONA Dental Systems GmbH, registered in EUDAMED on 19 Oct 2026 (Basic UDI-DI ++E276LEDviewPlusV017V) and listed in FDA GUDID since 10 Sep 2016 (UDI-DI +E27664814640), 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 Number++E276LEDviewPlusV017V Basic UDI-DI +E27664814640UDI-DIDate19 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number+E27664814640 UDI-DI Date10 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++E276LEDviewPlusV017V registered 19 Oct 2026 Active
  • FDA GUDID UDI-DI +E27664814640 listed 10 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID +E27664814640
  2. Registered EUDAMED ++E276LEDviewPlusV017V

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  • Withdrawn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
LEDview plus
Generic name
LED dental light, line-powered
Model / reference
6481464
Primary DI / UDI-DI
+E27664814640 EUDAMED
E27664814640 GUDID
Basic UDI-DI
++E276LEDviewPlusV017V
FDA product code
EAZ
EMDN code
Z12010701 Fixed scialytic lamps
GMDN term
LED dental light, line-powered
Device class
Class I
Regulation number
872.4630
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
+E27664814640
GUDID
E27664814640

The registries describe this device under different primary UDI-DIs (EUDAMED lists +E27664814640; FDA GUDID lists E27664814640), so their flags are not compared.

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)