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Stella 7 kg

EUDAMED

Class I (EU MDR)

Ref 735008131STS4Model Fiber Futon Stella

by Novista of Sweden AB

Identity

Trade Name
Stella 7 kg EUDAMED
Device Name
Fiber Futon Stella EUDAMED
Model / Reference
Fiber Futon Stella EUDAMED
735008131STS4 EUDAMED

Identifiers

Primary DI / UDI-DI
07350081310578 EUDAMED
Basic UDI-DI
735008131STS4 EUDAMED
Direct Marketing DI
07350081310578 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Stella 7 kg by Novista of Sweden AB — 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

EUDAMED SRN
SE-MF-000045071

Sources (1)

  • EUDAMED 3c08858c-acf9-4c41-a552-ebae788f6e9c 61 fields · synced Jun 18, 2026