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Fissurit F

EUDAMED

Class IIa (EU MDR)

Ref 1180Ref 1293Ref 1292

by VOCO GmbH

Identity

Trade Name
Fissurit F EUDAMED
Device Name
Fissurit F EUDAMED
Model / Reference
1180 EUDAMED
1293 EUDAMED
1292 EUDAMED

Identifiers

Primary DI / UDI-DI
E22111801 EUDAMED
E22112931 EUDAMED
E22112921 EUDAMED
Basic UDI-DI
++E22101500100000008L EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Fissurit F by VOCO GmbH — Class IIa — 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/MDR

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Manufacturer

Manufacturer
VOCO GmbH
EUDAMED SRN
DE-MF-000008601

Sources (3)

  • EUDAMED 89f126a0-8379-49d8-a099-7f3a24ac4a98 61 fields · synced Oct 6, 2026
  • EUDAMED 86a3b179-83bd-4c09-b7eb-1e183e24f01c 61 fields · synced Jul 10, 2026
  • EUDAMED d3dd9e3a-1c0f-4d3e-872e-1b2f28dcabe5 61 fields · synced Jul 13, 2026