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Cubeholter WS

EUDAMED

Class IIa (EU MDR)

Ref 85039510

by CARDIOLINE SpA

Identity

Device Name
Cubeholter WS EUDAMED
Model / Reference
85039510 EUDAMED

Identifiers

Primary DI / UDI-DI
08056732653009 EUDAMED
Basic UDI-DI
B-08056732653009 EUDAMED
EMDN Code
Z12050482 HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - 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

Cubeholter WS 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 5a83b7eb-f055-4351-9289-cc8ad698870c 61 fields · synced Jul 12, 2026