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Fisiowave

EUDAMED

Class IIb (EU MDR)

Ref FISIOWAVER2Model FISIOWAVE

by Fisioline Srl

Identity

Trade Name
FISIOWAVE EUDAMED
Model / Reference
FISIOWAVE EUDAMED
FISIOWAVER2 EUDAMED

Identifiers

Primary DI / UDI-DI
08057949170662 EUDAMED
Basic UDI-DI
B-08057949170662 EUDAMED
EMDN Code
Z120608 MICROWAVE THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIb 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Microwave ablation system probe, non-powered

Fisiowave by Fisioline Srl — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Fisioline Srl
EUDAMED SRN
IT-MF-000027924

Sources (1)

  • EUDAMED b67db434-23d9-445a-b67d-97cda326d266 61 fields · synced Jun 19, 2026