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Kołdra obciążeniowa

EUDAMED

Class I (EU MDR)

Ref KO100AM

by Action Spółka Akcyjna

Identity

Trade Name
Kołdra obciążeniowa EUDAMED
Device Name
Kołdra obciążeniowa EUDAMED
Model / Reference
KO100AM EUDAMED

Identifiers

Primary DI / UDI-DI
05901443410850 EUDAMED
Basic UDI-DI
5901443KOT5 EUDAMED
Direct Marketing DI
05901443410850 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

Kołdra obciążeniowa by Action Spółka Akcyjna — 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
PL-MF-000046182

Sources (1)

  • EUDAMED e4bdbcc9-15b3-45aa-9025-7c918a063bd0 61 fields · synced Jun 20, 2026