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Gel Demineralizant

EUDAMED

Class IIa (EU MDR)

Ref #314100

by Spident

Identity

Trade Name
Gel Demineralizant EUDAMED
Device Name
FineEtch EUDAMED
Model / Reference
#314100 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911115894 EUDAMED
Basic UDI-DI
B-08809911115894 EUDAMED
EMDN Code
Q01010402 ENAMEL-DENTINAL ETCHING MATERIALS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Gel Demineralizant by Spident — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

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 494c4e9f-f7d6-42c6-afa2-d2609684efbb 61 fields · synced Jul 28, 2026