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Kozetka lekarska

EUDAMED

Class I (EU MDR)

Ref SK85010

by Tribo sp. z o.o.

Identity

Trade Name
Kozetka lekarska EUDAMED
Device Name
Kozetka lekarska EUDAMED
Model / Reference
SK85010 EUDAMED

Identifiers

Primary DI / UDI-DI
59051413460017 EUDAMED
Basic UDI-DI
5905141346SK850104Y EUDAMED
Direct Marketing DI
59051413460017 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Kozetka lekarska by Tribo sp. z o.o. — 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
Tribo sp. z o.o.
EUDAMED SRN
PL-MF-000026942

Sources (1)

  • EUDAMED 660ab56d-6ac0-45bf-ba23-1316a40d27c3 61 fields · synced Jul 22, 2026