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DenFil BulkFlow

by Vericom Co., Ltd. 30 variants

Ref BR103-RA2N

DenFil BulkFlow (BR103-RA2N) is a Class IIa device made by Vericom Co., Ltd., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-08800123800714), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800123800714 Basic UDI-DI 08800123800714UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Light-cured radiopaque flowable composite resin
Model / reference
BR103-RA2N
Primary DI / UDI-DI
08800123800714
Basic UDI-DI
B-08800123800714
EMDN code
Q01010103 Dental restorative composites
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
KR-MF-000012442
Authorised representative
KTR Europe GmbH DE-AR-000005685

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
Other properties (11, all answered No)