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Oks 3000

EUDAMED

Class I (EU MDR)

Ref 0203 000x

by Integral Medical GmbH

Identity

Trade Name
OKS 3000 EUDAMED
Device Name
OKS 3000 EUDAMED
Model / Reference
0203 000x EUDAMED

Identifiers

Primary DI / UDI-DI
04262357040061 EUDAMED
Basic UDI-DI
426235704OKS30009J EUDAMED
Direct Marketing DI
04262357040061 EUDAMED
EMDN Code
Z11030503 PATIENT TABLES FOR RADIOLOGICAL EQUIPMENT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Oks 3000 by Integral Medical GmbH — 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

EUDAMED SRN
DE-MF-000006198

Sources (1)

  • EUDAMED 8b70c66e-263a-4805-85d4-bd27a3e4b7cc 61 fields · synced Jun 19, 2026