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Fcb7520/Mediberg

EUDAMED

Class I (EU MDR)

Ref FCB7520/MEDIBERGModel Sponge, disposable item for electrosurgery

by FIAB S.p.A.

Identity

Model / Reference
Sponge, disposable item for electrosurgery EUDAMED
FCB7520/MEDIBERG EUDAMED

Identifiers

Primary DI / UDI-DI
18054751930337 EUDAMED
Basic UDI-DI
803300326206000006NP EUDAMED
EMDN Code
K0299 ELECTROSURGERY DEVICES, SINGLE-USE - OTHER 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

Category: Percutaneous radio-frequency ablation system generator

Fcb7520/Mediberg by FIAB S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation system generator.

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 225cf702-c690-455c-a54c-d05cbbdb1acd 61 fields · synced Jul 14, 2026