← Back to catalogue

VioPaste

EUDAMED

Class IIa (EU MDR)

Ref #440200

by Spident

Identity

Trade Name
VioPaste EUDAMED
Device Name
VioPaste EUDAMED
Model / Reference
#440200 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262954364 EUDAMED
Basic UDI-DI
B-08809262954364 EUDAMED
EMDN Code
Q01010201 ROOT CANAL FILLING DENTAL PASTES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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

VioPaste 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 410f8bb0-b4e3-49ce-a600-d034fe1d7a50 61 fields · synced Aug 2, 2026