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F3010

EUDAMED

Class I (EU MDR)

Ref F3010Model Fully gelled electrodes for neurostimulation, bioimpedantiometry and EMG

by FIAB S.p.A.

Identity

Model / Reference
Fully gelled electrodes for neurostimulation, bioimpedantiometry and EMG EUDAMED
F3010 EUDAMED

Identifiers

Primary DI / UDI-DI
08033695721907 EUDAMED
Basic UDI-DI
803300326117000001NS EUDAMED
EMDN Code
N010101 ELECTROMYOGRAPHIC ELECTRODES EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

F3010 by FIAB S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
FIAB S.p.A.
EUDAMED SRN
IT-MF-000005988

Sources (1)

  • EUDAMED eb91e5f3-1b85-4259-8af7-2f43e49fa447 61 fields · synced Jun 18, 2026