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Logiq

EUDAMED

Class IIa (EU MDR)

Ref LOGIQ e SModel LOGIQ e

by GE Medical Systems CO. Ltd

Identity

Trade Name
LOGIQ EUDAMED
Device Name
LOGIQ e EUDAMED
Model / Reference
LOGIQ e EUDAMED
LOGIQ e S EUDAMED

Identifiers

Primary DI / UDI-DI
00198953078716 EUDAMED
Basic UDI-DI
8406821BUG00379J2 EUDAMED
Direct Marketing DI
00198953078716 EUDAMED
EMDN Code
Z11040103 PORTABLE ULTRASOUND SCANNERS EUDAMED

Classification

Device Class
Class IIa 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Logiq by GE Medical Systems CO. Ltd — Class IIa — 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
CN-MF-000001856
Authorised Representative
GE Medical Systems SCS FR-AR-000000344

Sources (1)

  • EUDAMED 8ad54099-01cf-4cc6-b337-aa101397e702 61 fields · synced May 23, 2026