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Rete Fisiosan Ibt

EUDAMED

Class I (EU MDR)

Ref FIELESCO100190

by DF MEDICA Oone srl

Identity

Trade Name
RETE FISIOSAN IBT EUDAMED
Device Name
RETI A SNODI ELETTRICI EUDAMED
Model / Reference
FIELESCO100190 EUDAMED

Identifiers

Primary DI / UDI-DI
08056994984279 EUDAMED
Basic UDI-DI
805699498FT009DORJ EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS 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

Rete Fisiosan Ibt by DF MEDICA Oone srl — 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
DF MEDICA Oone srl
EUDAMED SRN
IT-MF-000028375

Sources (1)

  • EUDAMED 2ccdf605-c796-4917-8e1f-474bd137af7e 61 fields · synced Jun 18, 2026