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Reticle Siemens

EUDAMED

Class I (EU MDR)

Ref 54-227Model Reticle Siemens

by Aktina Medical Corp

Identity

Trade Name
Reticle Siemens EUDAMED
Device Name
ROCR Reticule EUDAMED
Model / Reference
Reticle Siemens EUDAMED
54-227 EUDAMED

Identifiers

Primary DI / UDI-DI
+B365542270 EUDAMED
Basic UDI-DI
++B365SIEMENSACCES95 EUDAMED
Direct Marketing DI
+B365542270 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 (1)

  • EUDAMED 19628024-c245-4066-a7f4-e8a9e5115617 61 fields · synced Jun 18, 2026