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Smooff Rökavvänjning

EUDAMED

Class I (EU MDR)

Ref 224601

by SmokeQuit ApS

Identity

Trade Name
Smooff Rökavvänjning EUDAMED
Device Name
Smooff Rygestop EUDAMED
Model / Reference
224601 EUDAMED

Identifiers

Primary DI / UDI-DI
05700002009043 EUDAMED
Basic UDI-DI
57000022242SMOOFF001WQ 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

Smooff Rökavvänjning by SmokeQuit ApS — 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
SmokeQuit ApS
EUDAMED SRN
DK-MF-000019509

Sources (1)

  • EUDAMED 4b45f46d-c773-4753-b4b4-3a32140c8d74 61 fields · synced Jul 10, 2026