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Cubestress

EUDAMED

Class IIa (EU MDR)

Ref 85050100

by CARDIOLINE SpA

Identity

Device Name
Cubestress EUDAMED
Model / Reference
85050100 EUDAMED

Identifiers

Primary DI / UDI-DI
08056732653047 EUDAMED
Basic UDI-DI
B-08056732653047 EUDAMED
EMDN Code
Z12050182 STRESS ANALYSIS INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
-1192 EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Cubestress by Cardioline Spa — 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
CARDIOLINE SpA
EUDAMED SRN
IT-MF-000029682

Sources (1)

  • EUDAMED 038f131e-e8ca-478e-a5ba-6fdb1a23a67a 61 fields · synced Jun 19, 2026