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Logiq F

EUDAMED

Class IIa (EU MDR)

Ref 5976240Model LOGIQ F

by GE Medical Systems CO. Ltd

Identity

Device Name
LOGIQ F EUDAMED
Model / Reference
LOGIQ F EUDAMED
5976240 EUDAMED

Identifiers

Primary DI / UDI-DI
00198953037294 EUDAMED
Basic UDI-DI
08406821BUG004957R EUDAMED
EMDN Code
Z11040101 INTERNAL ULTRASOUND SCANNERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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 F 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 7c0f0c80-d403-442c-a384-8c7a64995271 61 fields · synced May 23, 2026