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Neo City

EUDAMED

Class IIa (EU MDR)

Ref 06429810585080Model NEO CITY Ref 0202

by Fimet Oy

Identity

Trade Name
NEO CITY EUDAMED
Device Name
NEO CITY EUDAMED
Dental Treatment System Fimet EUDAMED
Model / Reference
NEO CITY EUDAMED
06429810585080 EUDAMED
0202 EUDAMED

Identifiers

Primary DI / UDI-DI
06429810585080 EUDAMED
Basic UDI-DI
B-06429810585080 EUDAMED
6429810585dentalsystem5A EUDAMED
Direct Marketing DI
06429810585080 EUDAMED
EMDN Code
Z12110101 DENTAL TREATMENT UNITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Neo City by Fimet Oy — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Fimet Oy
EUDAMED SRN
FI-MF-000006831

Sources (2)

  • EUDAMED a988e3ef-7333-49dc-8205-b418bd39449c 61 fields · synced Jul 29, 2026
  • EUDAMED 6aecc75b-742e-4301-9417-adb84ffd2a4d 61 fields · synced May 19, 2026