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T Core

EUDAMED

Class IIa (EU MDR)

Ref FP1004KitModel T Core Kit

by Nexobio Co., Ltd.

Identity

Device Name
T Core EUDAMED
Model / Reference
T Core Kit EUDAMED
FP1004Kit EUDAMED

Identifiers

Primary DI / UDI-DI
08800032400821 EUDAMED
Basic UDI-DI
B-08800032400821 EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

T Core by Nexobio Co., Ltd. — 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
Nexobio Co., Ltd.
EUDAMED SRN
KR-MF-000043543
Authorised Representative
Mega Diş Deposu /Mustafa Soydan-Mete Yılmaz TR-AR-000040213

Sources (1)

  • EUDAMED 571ea8ee-f780-42ec-a6c8-679647f8897f 61 fields · synced Jun 18, 2026