Skip to content

EsFlow PLUS Injectable BW

by Spident 3 variants

Part of a family of 71 devices: see the family page

Ref #3306BA2P02

EsFlow PLUS Injectable BW (#3306BA2P02) is a Class IIa device made by Spident, registered in EUDAMED on 28 May 2026 (Basic UDI-DI 880926295SEPUB), active as of 23 Oct 2026.

Active European Union

CE MDR

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880926295SEPUB Basic UDI-DI 08809262950656UDI-DIDate28 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
EsFlow PLUS
Model / reference
#3306BA2P02
Primary DI / UDI-DI
08809262950656
Basic UDI-DI
880926295SEPUB
Direct marketing DI
08809262950656
EMDN code
Q01010103 Dental restorative composites
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
KR-MF-000008691
Authorised representative
AR Experts B.V. NL-AR-000023989

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from Spident

See all devices from Spident →

Properties

  • Implantable
Other properties (13, all answered No)