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ToDent Flow A1

EUDAMED

Class IIa (EU MDR)

Ref 39 05 05

by Spident

Identity

Trade Name
ToDent Flow A1 EUDAMED
Device Name
EsFlow EUDAMED
Model / Reference
39 05 05 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911112268 EUDAMED
Basic UDI-DI
880926295FI23 EUDAMED
B-08809911112268 EUDAMED
Direct Marketing DI
08809911112268 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 A1 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 69729f8e-e169-4f8e-b925-923cb5754299 61 fields · synced Jul 18, 2026
  • EUDAMED 701ad670-7b41-4c7a-9066-858d7ca133be 61 fields · synced Jul 17, 2026