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ToDent Flow A2

EUDAMED

Class IIa (EU MDR)

Ref 39 05 10

by Spident

Identity

Trade Name
ToDent Flow A2 EUDAMED
Device Name
EsFlow EUDAMED
Model / Reference
39 05 10 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911112275 EUDAMED
Basic UDI-DI
880926295FI23 EUDAMED
B-08809911112275 EUDAMED
Direct Marketing DI
08809911112275 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

Category: Dental composite resin

ToDent Flow A2 by Spident — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

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 4251e994-cc3b-4a40-a488-c990699bfc11 61 fields · synced Jul 23, 2026
  • EUDAMED 365d3823-e421-447a-8233-bd610e26a383 61 fields · synced Jul 23, 2026