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Stuoia Biosintesi

EUDAMED

Class I (EU MDR)

Ref BSW25

by DF MEDICA Oone srl

Identity

Trade Name
STUOIA BIOSINTESI EUDAMED
Device Name
DISPOSITIVI PER MAGNETOTERAPIA EUDAMED
Model / Reference
BSW25 EUDAMED

Identifiers

Primary DI / UDI-DI
08056994983098 EUDAMED
Basic UDI-DI
805699498FT006DOR3 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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: Device sterilization/disinfection container, reusable

Stuoia Biosintesi by DF MEDICA Oone srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

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 22237501-43de-4f86-bbad-bd204f706517 61 fields · synced Jun 18, 2026