← Back to catalogue

CardiMax FX-8300

EUDAMED

Class IIa (EU MDR)

Ref FX-8300

by Fukuda Denshi Co., Ltd.

Identity

Trade Name
CardiMax FX-8300 EUDAMED
Device Name
Electrocardiograph EUDAMED
Model / Reference
FX-8300 EUDAMED

Identifiers

Primary DI / UDI-DI
04538612914287 EUDAMED
Basic UDI-DI
4538612010009E EUDAMED
EMDN Code
Z12050301 GENERAL PURPOSE ELECTROCARDIOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

CardiMax FX-8300 by Fukuda Denshi Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
JP-MF-000008253
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 6302dc6b-15f0-4158-a5a9-0aa9202e9ef4 61 fields · synced Jul 10, 2026