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Dual Core DC118-M0BL

by Vericom Co., Ltd.

Ref DC118-M0BL

Dual Core DC118-M0BL is a device classified as Class IIa in the EU and Class II in the US made by Vericom Co., Ltd., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-08809254452571) and listed in FDA GUDID since 27 May 2026 (UDI-DI 08809254452571), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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/MDD EUDAMED NumberB-08809254452571 Basic UDI-DI 08809254452571UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08809254452571 UDI-DI Date27 May 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08809254452571 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 08809254452571 listed 27 May 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08809254452571
  2. Registered EUDAMED B-08809254452571

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Dual Core
Generic name
Dental composite resin
Device name
Dual-cured composite resin
Model / reference
DC118-M0BL
Primary DI / UDI-DI
08809254452571
Basic UDI-DI
B-08809254452571
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
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
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.

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from Vericom Co., Ltd.

See all devices from Vericom Co., Ltd. →

Properties

  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)