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Flow A2

by Spident

Part of a family of 25 devices: see the family page

Ref Ρ982

Flow A2 (Ρ982) is a Class IIa device made by Spident, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 880926295FI23), active as of 22 Oct 2026.

Active European Union

CE MDR 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number880926295FI23 Basic UDI-DI 08809911112381UDI-DIDate5 Jun 2026RegisteredStatusActive
European UnionCE/MDR Number880926295FI23 Basic UDI-DI 08809911112381UDI-DIDate5 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
EsFlow
Model / reference
Ρ982
Primary DI / UDI-DI
08809911112381
Basic UDI-DI
880926295FI23, B-08809911112381
Direct marketing DI
08809911112381
EMDN code
Q01010103 Dental restorative composites
Device class
Class IIa
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Spain
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)