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ToDent Flow A3.5

EUDAMED

Class IIa (EU MDR)

Ref 39 05 20

by Spident

Identity

Trade Name
ToDent Flow A3.5 EUDAMED
Device Name
EsFlow EUDAMED
Model / Reference
39 05 20 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911112299 EUDAMED
Basic UDI-DI
880926295FI23 EUDAMED
B-08809911112299 EUDAMED
Direct Marketing DI
08809911112299 EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED
Greece EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ToDent Flow A3.5 by Spident — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Spident
EUDAMED SRN
KR-MF-000008691
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 8b1e0878-e469-40d1-ae06-a5ce3dee9e5c 61 fields · synced Jul 23, 2026
  • EUDAMED 7b430879-dd3d-417b-8202-f003f0e71903 61 fields · synced Jul 23, 2026