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ToDent Core Dual

EUDAMED

Class IIa (EU MDR)

Ref 39 00 05

by Spident

Identity

Trade Name
ToDent Core Dual EUDAMED
Device Name
Core it Dual EUDAMED
Model / Reference
39 00 05 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911112336 EUDAMED
Basic UDI-DI
B-08809911112336 EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Dental composite resin

ToDent Core Dual by Spident — Class IIa — MDD — 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

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Manufacturer

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

Sources (1)

  • EUDAMED 6a8410b2-a00a-4277-a881-ac32914e7a54 61 fields · synced Jul 11, 2026