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Lumix Q Platform

EUDAMED

Class IIb (EU MDR)

Ref LUMIXQ02

by Fisioline Srl

Identity

Trade Name
LUMIX Q PLATFORM EUDAMED
Device Name
LUMIX Q PLATFORM EUDAMED
Model / Reference
LUMIXQ02 EUDAMED

Identifiers

Primary DI / UDI-DI
08057949171652 EUDAMED
Basic UDI-DI
B-08057949171652 EUDAMED
EMDN Code
Z12011019 MULTI–PLATFORM LASER 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

Lumix Q Platform by Fisioline Srl — Class IIb — 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
Fisioline Srl
EUDAMED SRN
IT-MF-000027924

Sources (1)

  • EUDAMED 85acda2d-5246-40fc-91f3-906ef4ef0607 61 fields · synced Jun 18, 2026