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Reticle Siemens

EUDAMED

Class I (EU MDR)

Ref 54-224Model Reticle SiemensRef 54-225

by Aktina Medical Corp

Identity

Trade Name
Reticle Siemens EUDAMED
Device Name
ROCR Reticule EUDAMED
Model / Reference
Reticle Siemens EUDAMED
54-224 EUDAMED
54-225 EUDAMED

Identifiers

Primary DI / UDI-DI
+B365542240 EUDAMED
+B365542250 EUDAMED
Basic UDI-DI
++B365SIEMENSACCES95 EUDAMED
Direct Marketing DI
+B365542240 EUDAMED
+B365542250 EUDAMED
EMDN Code
Z11010199 LINEAR ACCELERATORS – OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Reticle Siemens by Aktina Medical Corp — 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
Aktina Medical Corp
EUDAMED SRN
US-MF-000005935
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (2)

  • EUDAMED 7509f0b6-0b2e-47d8-b92f-daeeea733419 61 fields · synced Oct 6, 2026
  • EUDAMED b7c6df11-dd67-49ca-94e6-6137b7440641 61 fields · synced May 19, 2026