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SkanSiesta

EUDAMED

Class IIb (EU MDR)

Ref F3-75-390-0240-56Model SkanSiesta

by Skanray Technologies Limited

Identity

Trade Name
SkanSiesta EUDAMED
Model / Reference
SkanSiesta EUDAMED
F3-75-390-0240-56 EUDAMED

Identifiers

Primary DI / UDI-DI
18904269465701 EUDAMED
Basic UDI-DI
B-18904269465701 EUDAMED
EMDN Code
Z1203010199 ANAESTHESIA SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

SkanSiesta by Skanray Technologies Limited — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000034819
Authorised Representative
SKANRAY EUROPE SRL IT-AR-000013034

Sources (1)

  • EUDAMED a54565e2-7a4b-4b42-a881-34863d503a2d 61 fields · synced Jul 25, 2026