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iControl

EUDAMED

Class I (EU MDR)

Ref iControl

by Pretorian Technologies Ltd

Identity

Trade Name
iControl EUDAMED
Device Name
Tablet Access Devices EUDAMED
Model / Reference
iControl EUDAMED

Identifiers

Primary DI / UDI-DI
05060895630688 EUDAMED
Basic UDI-DI
506089563BTIFDA EUDAMED
Direct Marketing DI
05060895630688 EUDAMED
EMDN Code
Y210999 PERSONAL COMPUTER INPUT AND OUTPUT PERIPHERAL EQUIPMENT - OTHER 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

iControl 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 4db4da95-c00e-49b3-ad3c-7f23e5c4d9f5 61 fields · synced Oct 6, 2026