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iQ-LITE 3.1

EUDAMED

Class IIa (EU MDR)

Ref IQLITE31

by IMAGE Information Systems Europe GmbH

Identity

Trade Name
iQ-LITE 3.1 EUDAMED
Device Name
iQ-LITE 3.1 EUDAMED
Model / Reference
IQLITE31 EUDAMED

Identifiers

Primary DI / UDI-DI
D-DEMF000004979LITE31XP EUDAMED
Basic UDI-DI
B-DEMF000004979LITE31XP EUDAMED
EMDN Code
Z110603 PICTURE ARCHIVING AND COMMUNICATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
-1192 EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

iQ-LITE 3.1 by IMAGE INFORMATION SYSTEMS EUROPE GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000004979

Sources (1)

  • EUDAMED bc199ce1-2cfc-4f81-b8b1-167dcd05858d 61 fields · synced Jun 19, 2026