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n-ABLER Joystick

EUDAMED

Class I (EU MDR)

Ref n-ABLER Joystick

by Pretorian Technologies Ltd

Identity

Trade Name
n-ABLER Joystick EUDAMED
Device Name
Joysticks EUDAMED
Model / Reference
n-ABLER Joystick EUDAMED

Identifiers

Primary DI / UDI-DI
05060895630169 EUDAMED
Basic UDI-DI
506089563JSK1DT EUDAMED
Direct Marketing DI
05060895630169 EUDAMED
EMDN Code
Y210906 MOUSE AND KEYBOARD EMULATORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

n-ABLER Joystick by Pretorian Technologies Ltd — 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
GB-MF-000008344
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED d6255e0f-09ab-456a-8f27-54feae70ace4 61 fields · synced Jun 20, 2026