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TomoCon GO 3.0

EUDAMED

Class IIa (EU MDR)

Ref TomoCon GO 3.0

by TatraMed Software s.r.o.

Identity

Trade Name
TomoCon GO 3.0 EUDAMED
Device Name
TomoCon GO EUDAMED
Model / Reference
TomoCon GO 3.0 EUDAMED

Identifiers

Primary DI / UDI-DI
08588008910023 EUDAMED
Basic UDI-DI
8588008910-TomoConGO-DA EUDAMED
Direct Marketing DI
08588008910023 EUDAMED
EMDN Code
Z11069005 DIAGNOSTIC IMAGING WORKSTATIONS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Slovakia 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

TomoCon GO 3.0 by TatraMed Software s.r.o. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
SK-MF-000017681

Sources (1)

  • EUDAMED 62081fee-5f55-405e-9ab2-0b4d1e85341a 61 fields · synced Jul 28, 2026