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Patient fiducial - Marker kit

EUDAMED

Class I (EU MDR)

Ref MK000

by R.A.W. Srl

Identity

Trade Name
Patient fiducial - Marker kit EUDAMED
Device Name
Patient fiducial - Marker kit EUDAMED
Model / Reference
MK000 EUDAMED

Identifiers

Primary DI / UDI-DI
08052141890080 EUDAMED
Basic UDI-DI
8052141890004MK00ED EUDAMED
Direct Marketing DI
08052141890080 EUDAMED
EMDN Code
Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Patient fiducial - Marker kit by R.A.W. Srl — 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
R.A.W. Srl
EUDAMED SRN
IT-MF-000027589

Sources (1)

  • EUDAMED 1c2162ac-a002-4843-aed1-4b6d9fcd8f32 61 fields · synced Jun 18, 2026