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SteadyBody pussilakana 240x220 harmaa

EUDAMED

Class I (EU MDR)

Ref LAKSTE240PLHA

by Group Unikulma Oy

Identity

Trade Name
SteadyBody pussilakana 240x220 harmaa EUDAMED
Device Name
SBTL EUDAMED
Model / Reference
LAKSTE240PLHA EUDAMED

Identifiers

Primary DI / UDI-DI
06430024153941 EUDAMED
Basic UDI-DI
643002415SBLAK2F EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

SteadyBody pussilakana 240x220 harmaa by Group Unikulma Oy — 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
Group Unikulma Oy
EUDAMED SRN
FI-MF-000016906

Sources (1)

  • EUDAMED e93822b2-28fa-4f28-8ba9-376b14e07871 61 fields · synced Jun 18, 2026