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Alisei Fissa

EUDAMED

Class I (EU MDR)

Ref R21ALIF

by Sogno Veneto S.p.A.

Identity

Trade Name
ALISEI FISSA EUDAMED
Device Name
ALISEI FISSA EUDAMED
Model / Reference
R21ALIF EUDAMED

Identifiers

Primary DI / UDI-DI
08054726762690 EUDAMED
Basic UDI-DI
805472676269FT EUDAMED
EMDN Code
V080699 MEDICAL BEDS - 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

Alisei Fissa by Sogno Veneto 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
Sogno Veneto S.p.A.
EUDAMED SRN
IT-MF-000048125

Sources (1)

  • EUDAMED 939a0cb3-a815-44c7-9106-9b4bad729810 61 fields · synced Jul 22, 2026