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Xpert20

EUDAMED

Class I (EU MDR)

Ref XPERT20

by Kub Technologies Inc

Identity

Trade Name
XPERT20 EUDAMED
Device Name
XPERT Series Tissue Specimen X-ray System EUDAMED
Model / Reference
XPERT20 EUDAMED

Identifiers

Primary DI / UDI-DI
+B619X201I EUDAMED
Basic UDI-DI
++B619XSERIESBC EUDAMED
Direct Marketing DI
+B619X201I EUDAMED
EMDN Code
Z11031101 MULTIFUNCTIONAL SYSTEMS FOR DIRECT DIGITAL RADIOLOGY 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: Stationary basic diagnostic x-ray system, digital

Xpert20 by Kub Technologies Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000026338
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 93576f8e-5faf-449b-b96d-320472c06d7f 61 fields · synced Jul 9, 2026