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BRIGHT LIGHT C2, 0.25g x 20

by Dmp Dental Industry S.A.

Part of a family of 340 devices: see the family page

Ref 110122512

BRIGHT LIGHT C2, 0.25g x 20 (110122512) is a device classified as Class IIa in the EU and Class II in the US made by Dmp Dental Industry S.A., registered in EUDAMED on 22 May 2026 (Basic UDI-DI 5206569COMP42SA) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 05206569895124), 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 Number5206569COMP42SA Basic UDI-DI 05206569895124UDI-DIDate22 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05206569895124 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 5206569COMP42SA registered 22 May 2026 Active
  • FDA GUDID UDI-DI 05206569895124 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05206569895124
  2. Registered EUDAMED 5206569COMP42SA

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  • Withdrawn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
Bright Light 0.25g x 20 C2 EUDAMED
Bright Light GUDID
Generic name
Dental composite resin
Device name
Light Curing Microhybrid Composite
Model / Ref / Catalog
110122512, C2, 0.25g x 20
Primary DI / UDI-DI
05206569895124
Basic UDI-DI
5206569COMP42SA
FDA product code
EBF
EMDN code
Q01010103 Dental restorative composites
GMDN term
Dental composite resin
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3690
EU registration type
Standard device
EU market of registration
Greece
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
110122512
GUDID
C2, 0.25g x 20
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

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: Dental composite resin

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from Dmp Dental Industry S.A.

See all devices from Dmp Dental Industry S.A. →

Properties

  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)